Name: rs11377789
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs11377789

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:11528826-11528846 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₃ / del(A)₁₂ / del(A)₉ / de…
del(A)₁₃ / del(A)₁₂ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.000004 (1/264690, TOPMED)
del(A)₁₃=0.0000 (0/5864, ALFA)
del(A)₁₂=0.0000 (0/5864, ALFA) (+ 11 more)
del(A)₉=0.0000 (0/5864, ALFA)
del(A)₇=0.0000 (0/5864, ALFA)
del(A)₆=0.0000 (0/5864, ALFA)
del(A)₄=0.0000 (0/5864, ALFA)
delAAA=0.0000 (0/5864, ALFA)
delAA=0.0000 (0/5864, ALFA)
delA=0.0000 (0/5864, ALFA)
dupA=0.0000 (0/5864, ALFA)
dupAA=0.0000 (0/5864, ALFA)
dupAAA=0.0000 (0/5864, ALFA)
delAA=0.2238 (1121/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ATG7 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	5864	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	5106	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	386	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	14	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	372	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	40	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	32	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	38	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	124	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	32	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	138	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₁=0.999996	del(A)₁₃=0.000004
Allele Frequency Aggregator	Total	Global	5864	(A)₂₁=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	5106	(A)₂₁=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	386	(A)₂₁=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	138	(A)₂₁=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	124	(A)₂₁=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Asian	Sub	40	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	38	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(A)₂₁=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₂₁=0.7762	delAA=0.2238
1000Genomes	African	Sub	1322	(A)₂₁=0.6006	delAA=0.3994
1000Genomes	East Asian	Sub	1008	(A)₂₁=0.8829	delAA=0.1171
1000Genomes	Europe	Sub	1006	(A)₂₁=0.7485	delAA=0.2515
1000Genomes	South Asian	Sub	978	(A)₂₁=0.904	delAA=0.096
1000Genomes	American	Sub	694	(A)₂₁=0.816	delAA=0.184

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.11528834_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528835_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528838_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528839_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528840_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528841_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528842_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528843_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528844_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528845_11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528846del
GRCh38.p14 chr 3	NC_000003.12:g.11528846dup
GRCh38.p14 chr 3	NC_000003.12:g.11528845_11528846dup
GRCh38.p14 chr 3	NC_000003.12:g.11528844_11528846dup
GRCh38.p14 chr 3	NC_000003.12:g.11528843_11528846dup
GRCh38.p14 chr 3	NC_000003.12:g.11528842_11528846dup
GRCh37.p13 chr 3	NC_000003.11:g.11570308_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570309_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570312_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570313_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570314_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570315_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570316_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570317_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570318_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570319_11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570320del
GRCh37.p13 chr 3	NC_000003.11:g.11570320dup
GRCh37.p13 chr 3	NC_000003.11:g.11570319_11570320dup
GRCh37.p13 chr 3	NC_000003.11:g.11570318_11570320dup
GRCh37.p13 chr 3	NC_000003.11:g.11570317_11570320dup
GRCh37.p13 chr 3	NC_000003.11:g.11570316_11570320dup

Gene: ATG7, autophagy related 7 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ATG7 transcript variant 2	NM_001136031.3:c.1999-259… NM_001136031.3:c.1999-25977_1999-25965del	N/A	Intron Variant
ATG7 transcript variant 3	NM_001144912.2:c.1840-259… NM_001144912.2:c.1840-25977_1840-25965del	N/A	Intron Variant
ATG7 transcript variant 4	NM_001349232.2:c.2080-259… NM_001349232.2:c.2080-25977_2080-25965del	N/A	Intron Variant
ATG7 transcript variant 5	NM_001349233.2:c.2080-259… NM_001349233.2:c.2080-25977_2080-25965del	N/A	Intron Variant
ATG7 transcript variant 6	NM_001349234.2:c.2080-259… NM_001349234.2:c.2080-25977_2080-25965del	N/A	Intron Variant
ATG7 transcript variant 7	NM_001349235.2:c.2080-259… NM_001349235.2:c.2080-25977_2080-25965del	N/A	Intron Variant
ATG7 transcript variant 8	NM_001349236.2:c.1963-259… NM_001349236.2:c.1963-25977_1963-25965del	N/A	Intron Variant
ATG7 transcript variant 9	NM_001349237.2:c.1921-259… NM_001349237.2:c.1921-25977_1921-25965del	N/A	Intron Variant
ATG7 transcript variant 10	NM_001349238.2:c.1147-354… NM_001349238.2:c.1147-35425_1147-35413del	N/A	Intron Variant
ATG7 transcript variant 1	NM_006395.3:c.2080-25977_… NM_006395.3:c.2080-25977_2080-25965del	N/A	Intron Variant
ATG7 transcript variant X27	XM_047447308.1:c.1462-259… XM_047447308.1:c.1462-25977_1462-25965del	N/A	Intron Variant
ATG7 transcript variant X1	XM_006712931.5:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X12	XM_006712932.5:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X10	XM_011533277.4:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X15	XM_017005542.2:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X17	XM_017005543.2:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X6	XM_017005548.2:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X19	XM_017005550.2:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X20	XM_017005551.2:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X2	XM_024453312.2:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X3	XM_047447293.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X7	XM_047447294.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X8	XM_047447295.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X9	XM_047447296.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X11	XM_047447297.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X13	XM_047447298.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X14	XM_047447299.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X16	XM_047447300.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X18	XM_047447301.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X21	XM_047447302.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X22	XM_047447303.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X23	XM_047447304.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X24	XM_047447305.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X25	XM_047447306.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X26	XM_047447307.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X28	XM_047447309.1:c.	N/A	Genic Downstream Transcript Variant
ATG7 transcript variant X4	XR_007095622.1:n.	N/A	Intron Variant
ATG7 transcript variant X5	XR_007095623.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₂₁=	del(A)₁₃	del(A)₁₂	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 3	NC_000003.12:g.11528826_11528846=	NC_000003.12:g.11528834_11528846del	NC_000003.12:g.11528835_11528846del	NC_000003.12:g.11528838_11528846del	NC_000003.12:g.11528839_11528846del	NC_000003.12:g.11528840_11528846del	NC_000003.12:g.11528841_11528846del	NC_000003.12:g.11528842_11528846del	NC_000003.12:g.11528843_11528846del	NC_000003.12:g.11528844_11528846del	NC_000003.12:g.11528845_11528846del	NC_000003.12:g.11528846del	NC_000003.12:g.11528846dup	NC_000003.12:g.11528845_11528846dup	NC_000003.12:g.11528844_11528846dup	NC_000003.12:g.11528843_11528846dup	NC_000003.12:g.11528842_11528846dup
GRCh37.p13 chr 3	NC_000003.11:g.11570300_11570320=	NC_000003.11:g.11570308_11570320del	NC_000003.11:g.11570309_11570320del	NC_000003.11:g.11570312_11570320del	NC_000003.11:g.11570313_11570320del	NC_000003.11:g.11570314_11570320del	NC_000003.11:g.11570315_11570320del	NC_000003.11:g.11570316_11570320del	NC_000003.11:g.11570317_11570320del	NC_000003.11:g.11570318_11570320del	NC_000003.11:g.11570319_11570320del	NC_000003.11:g.11570320del	NC_000003.11:g.11570320dup	NC_000003.11:g.11570319_11570320dup	NC_000003.11:g.11570318_11570320dup	NC_000003.11:g.11570317_11570320dup	NC_000003.11:g.11570316_11570320dup
ATG7 transcript variant 2	NM_001136031.2:c.1999-25985=	NM_001136031.2:c.1999-25977_1999-25965del	NM_001136031.2:c.1999-25976_1999-25965del	NM_001136031.2:c.1999-25973_1999-25965del	NM_001136031.2:c.1999-25972_1999-25965del	NM_001136031.2:c.1999-25971_1999-25965del	NM_001136031.2:c.1999-25970_1999-25965del	NM_001136031.2:c.1999-25969_1999-25965del	NM_001136031.2:c.1999-25968_1999-25965del	NM_001136031.2:c.1999-25967_1999-25965del	NM_001136031.2:c.1999-25966_1999-25965del	NM_001136031.2:c.1999-25965del	NM_001136031.2:c.1999-25965dup	NM_001136031.2:c.1999-25966_1999-25965dup	NM_001136031.2:c.1999-25967_1999-25965dup	NM_001136031.2:c.1999-25968_1999-25965dup	NM_001136031.2:c.1999-25969_1999-25965dup
ATG7 transcript variant 2	NM_001136031.3:c.1999-25985=	NM_001136031.3:c.1999-25977_1999-25965del	NM_001136031.3:c.1999-25976_1999-25965del	NM_001136031.3:c.1999-25973_1999-25965del	NM_001136031.3:c.1999-25972_1999-25965del	NM_001136031.3:c.1999-25971_1999-25965del	NM_001136031.3:c.1999-25970_1999-25965del	NM_001136031.3:c.1999-25969_1999-25965del	NM_001136031.3:c.1999-25968_1999-25965del	NM_001136031.3:c.1999-25967_1999-25965del	NM_001136031.3:c.1999-25966_1999-25965del	NM_001136031.3:c.1999-25965del	NM_001136031.3:c.1999-25965dup	NM_001136031.3:c.1999-25966_1999-25965dup	NM_001136031.3:c.1999-25967_1999-25965dup	NM_001136031.3:c.1999-25968_1999-25965dup	NM_001136031.3:c.1999-25969_1999-25965dup
ATG7 transcript variant 3	NM_001144912.1:c.1840-25985=	NM_001144912.1:c.1840-25977_1840-25965del	NM_001144912.1:c.1840-25976_1840-25965del	NM_001144912.1:c.1840-25973_1840-25965del	NM_001144912.1:c.1840-25972_1840-25965del	NM_001144912.1:c.1840-25971_1840-25965del	NM_001144912.1:c.1840-25970_1840-25965del	NM_001144912.1:c.1840-25969_1840-25965del	NM_001144912.1:c.1840-25968_1840-25965del	NM_001144912.1:c.1840-25967_1840-25965del	NM_001144912.1:c.1840-25966_1840-25965del	NM_001144912.1:c.1840-25965del	NM_001144912.1:c.1840-25965dup	NM_001144912.1:c.1840-25966_1840-25965dup	NM_001144912.1:c.1840-25967_1840-25965dup	NM_001144912.1:c.1840-25968_1840-25965dup	NM_001144912.1:c.1840-25969_1840-25965dup
ATG7 transcript variant 3	NM_001144912.2:c.1840-25985=	NM_001144912.2:c.1840-25977_1840-25965del	NM_001144912.2:c.1840-25976_1840-25965del	NM_001144912.2:c.1840-25973_1840-25965del	NM_001144912.2:c.1840-25972_1840-25965del	NM_001144912.2:c.1840-25971_1840-25965del	NM_001144912.2:c.1840-25970_1840-25965del	NM_001144912.2:c.1840-25969_1840-25965del	NM_001144912.2:c.1840-25968_1840-25965del	NM_001144912.2:c.1840-25967_1840-25965del	NM_001144912.2:c.1840-25966_1840-25965del	NM_001144912.2:c.1840-25965del	NM_001144912.2:c.1840-25965dup	NM_001144912.2:c.1840-25966_1840-25965dup	NM_001144912.2:c.1840-25967_1840-25965dup	NM_001144912.2:c.1840-25968_1840-25965dup	NM_001144912.2:c.1840-25969_1840-25965dup
ATG7 transcript variant 4	NM_001349232.2:c.2080-25985=	NM_001349232.2:c.2080-25977_2080-25965del	NM_001349232.2:c.2080-25976_2080-25965del	NM_001349232.2:c.2080-25973_2080-25965del	NM_001349232.2:c.2080-25972_2080-25965del	NM_001349232.2:c.2080-25971_2080-25965del	NM_001349232.2:c.2080-25970_2080-25965del	NM_001349232.2:c.2080-25969_2080-25965del	NM_001349232.2:c.2080-25968_2080-25965del	NM_001349232.2:c.2080-25967_2080-25965del	NM_001349232.2:c.2080-25966_2080-25965del	NM_001349232.2:c.2080-25965del	NM_001349232.2:c.2080-25965dup	NM_001349232.2:c.2080-25966_2080-25965dup	NM_001349232.2:c.2080-25967_2080-25965dup	NM_001349232.2:c.2080-25968_2080-25965dup	NM_001349232.2:c.2080-25969_2080-25965dup
ATG7 transcript variant 5	NM_001349233.2:c.2080-25985=	NM_001349233.2:c.2080-25977_2080-25965del	NM_001349233.2:c.2080-25976_2080-25965del	NM_001349233.2:c.2080-25973_2080-25965del	NM_001349233.2:c.2080-25972_2080-25965del	NM_001349233.2:c.2080-25971_2080-25965del	NM_001349233.2:c.2080-25970_2080-25965del	NM_001349233.2:c.2080-25969_2080-25965del	NM_001349233.2:c.2080-25968_2080-25965del	NM_001349233.2:c.2080-25967_2080-25965del	NM_001349233.2:c.2080-25966_2080-25965del	NM_001349233.2:c.2080-25965del	NM_001349233.2:c.2080-25965dup	NM_001349233.2:c.2080-25966_2080-25965dup	NM_001349233.2:c.2080-25967_2080-25965dup	NM_001349233.2:c.2080-25968_2080-25965dup	NM_001349233.2:c.2080-25969_2080-25965dup
ATG7 transcript variant 6	NM_001349234.2:c.2080-25985=	NM_001349234.2:c.2080-25977_2080-25965del	NM_001349234.2:c.2080-25976_2080-25965del	NM_001349234.2:c.2080-25973_2080-25965del	NM_001349234.2:c.2080-25972_2080-25965del	NM_001349234.2:c.2080-25971_2080-25965del	NM_001349234.2:c.2080-25970_2080-25965del	NM_001349234.2:c.2080-25969_2080-25965del	NM_001349234.2:c.2080-25968_2080-25965del	NM_001349234.2:c.2080-25967_2080-25965del	NM_001349234.2:c.2080-25966_2080-25965del	NM_001349234.2:c.2080-25965del	NM_001349234.2:c.2080-25965dup	NM_001349234.2:c.2080-25966_2080-25965dup	NM_001349234.2:c.2080-25967_2080-25965dup	NM_001349234.2:c.2080-25968_2080-25965dup	NM_001349234.2:c.2080-25969_2080-25965dup
ATG7 transcript variant 7	NM_001349235.2:c.2080-25985=	NM_001349235.2:c.2080-25977_2080-25965del	NM_001349235.2:c.2080-25976_2080-25965del	NM_001349235.2:c.2080-25973_2080-25965del	NM_001349235.2:c.2080-25972_2080-25965del	NM_001349235.2:c.2080-25971_2080-25965del	NM_001349235.2:c.2080-25970_2080-25965del	NM_001349235.2:c.2080-25969_2080-25965del	NM_001349235.2:c.2080-25968_2080-25965del	NM_001349235.2:c.2080-25967_2080-25965del	NM_001349235.2:c.2080-25966_2080-25965del	NM_001349235.2:c.2080-25965del	NM_001349235.2:c.2080-25965dup	NM_001349235.2:c.2080-25966_2080-25965dup	NM_001349235.2:c.2080-25967_2080-25965dup	NM_001349235.2:c.2080-25968_2080-25965dup	NM_001349235.2:c.2080-25969_2080-25965dup
ATG7 transcript variant 8	NM_001349236.2:c.1963-25985=	NM_001349236.2:c.1963-25977_1963-25965del	NM_001349236.2:c.1963-25976_1963-25965del	NM_001349236.2:c.1963-25973_1963-25965del	NM_001349236.2:c.1963-25972_1963-25965del	NM_001349236.2:c.1963-25971_1963-25965del	NM_001349236.2:c.1963-25970_1963-25965del	NM_001349236.2:c.1963-25969_1963-25965del	NM_001349236.2:c.1963-25968_1963-25965del	NM_001349236.2:c.1963-25967_1963-25965del	NM_001349236.2:c.1963-25966_1963-25965del	NM_001349236.2:c.1963-25965del	NM_001349236.2:c.1963-25965dup	NM_001349236.2:c.1963-25966_1963-25965dup	NM_001349236.2:c.1963-25967_1963-25965dup	NM_001349236.2:c.1963-25968_1963-25965dup	NM_001349236.2:c.1963-25969_1963-25965dup
ATG7 transcript variant 9	NM_001349237.2:c.1921-25985=	NM_001349237.2:c.1921-25977_1921-25965del	NM_001349237.2:c.1921-25976_1921-25965del	NM_001349237.2:c.1921-25973_1921-25965del	NM_001349237.2:c.1921-25972_1921-25965del	NM_001349237.2:c.1921-25971_1921-25965del	NM_001349237.2:c.1921-25970_1921-25965del	NM_001349237.2:c.1921-25969_1921-25965del	NM_001349237.2:c.1921-25968_1921-25965del	NM_001349237.2:c.1921-25967_1921-25965del	NM_001349237.2:c.1921-25966_1921-25965del	NM_001349237.2:c.1921-25965del	NM_001349237.2:c.1921-25965dup	NM_001349237.2:c.1921-25966_1921-25965dup	NM_001349237.2:c.1921-25967_1921-25965dup	NM_001349237.2:c.1921-25968_1921-25965dup	NM_001349237.2:c.1921-25969_1921-25965dup
ATG7 transcript variant 10	NM_001349238.2:c.1147-35433=	NM_001349238.2:c.1147-35425_1147-35413del	NM_001349238.2:c.1147-35424_1147-35413del	NM_001349238.2:c.1147-35421_1147-35413del	NM_001349238.2:c.1147-35420_1147-35413del	NM_001349238.2:c.1147-35419_1147-35413del	NM_001349238.2:c.1147-35418_1147-35413del	NM_001349238.2:c.1147-35417_1147-35413del	NM_001349238.2:c.1147-35416_1147-35413del	NM_001349238.2:c.1147-35415_1147-35413del	NM_001349238.2:c.1147-35414_1147-35413del	NM_001349238.2:c.1147-35413del	NM_001349238.2:c.1147-35413dup	NM_001349238.2:c.1147-35414_1147-35413dup	NM_001349238.2:c.1147-35415_1147-35413dup	NM_001349238.2:c.1147-35416_1147-35413dup	NM_001349238.2:c.1147-35417_1147-35413dup
ATG7 transcript variant 1	NM_006395.2:c.2080-25985=	NM_006395.2:c.2080-25977_2080-25965del	NM_006395.2:c.2080-25976_2080-25965del	NM_006395.2:c.2080-25973_2080-25965del	NM_006395.2:c.2080-25972_2080-25965del	NM_006395.2:c.2080-25971_2080-25965del	NM_006395.2:c.2080-25970_2080-25965del	NM_006395.2:c.2080-25969_2080-25965del	NM_006395.2:c.2080-25968_2080-25965del	NM_006395.2:c.2080-25967_2080-25965del	NM_006395.2:c.2080-25966_2080-25965del	NM_006395.2:c.2080-25965del	NM_006395.2:c.2080-25965dup	NM_006395.2:c.2080-25966_2080-25965dup	NM_006395.2:c.2080-25967_2080-25965dup	NM_006395.2:c.2080-25968_2080-25965dup	NM_006395.2:c.2080-25969_2080-25965dup
ATG7 transcript variant 1	NM_006395.3:c.2080-25985=	NM_006395.3:c.2080-25977_2080-25965del	NM_006395.3:c.2080-25976_2080-25965del	NM_006395.3:c.2080-25973_2080-25965del	NM_006395.3:c.2080-25972_2080-25965del	NM_006395.3:c.2080-25971_2080-25965del	NM_006395.3:c.2080-25970_2080-25965del	NM_006395.3:c.2080-25969_2080-25965del	NM_006395.3:c.2080-25968_2080-25965del	NM_006395.3:c.2080-25967_2080-25965del	NM_006395.3:c.2080-25966_2080-25965del	NM_006395.3:c.2080-25965del	NM_006395.3:c.2080-25965dup	NM_006395.3:c.2080-25966_2080-25965dup	NM_006395.3:c.2080-25967_2080-25965dup	NM_006395.3:c.2080-25968_2080-25965dup	NM_006395.3:c.2080-25969_2080-25965dup
ATG7 transcript variant X1	XM_005264800.1:c.2080-25985=	XM_005264800.1:c.2080-25977_2080-25965del	XM_005264800.1:c.2080-25976_2080-25965del	XM_005264800.1:c.2080-25973_2080-25965del	XM_005264800.1:c.2080-25972_2080-25965del	XM_005264800.1:c.2080-25971_2080-25965del	XM_005264800.1:c.2080-25970_2080-25965del	XM_005264800.1:c.2080-25969_2080-25965del	XM_005264800.1:c.2080-25968_2080-25965del	XM_005264800.1:c.2080-25967_2080-25965del	XM_005264800.1:c.2080-25966_2080-25965del	XM_005264800.1:c.2080-25965del	XM_005264800.1:c.2080-25965dup	XM_005264800.1:c.2080-25966_2080-25965dup	XM_005264800.1:c.2080-25967_2080-25965dup	XM_005264800.1:c.2080-25968_2080-25965dup	XM_005264800.1:c.2080-25969_2080-25965dup
ATG7 transcript variant X2	XM_005264801.1:c.2080-25985=	XM_005264801.1:c.2080-25977_2080-25965del	XM_005264801.1:c.2080-25976_2080-25965del	XM_005264801.1:c.2080-25973_2080-25965del	XM_005264801.1:c.2080-25972_2080-25965del	XM_005264801.1:c.2080-25971_2080-25965del	XM_005264801.1:c.2080-25970_2080-25965del	XM_005264801.1:c.2080-25969_2080-25965del	XM_005264801.1:c.2080-25968_2080-25965del	XM_005264801.1:c.2080-25967_2080-25965del	XM_005264801.1:c.2080-25966_2080-25965del	XM_005264801.1:c.2080-25965del	XM_005264801.1:c.2080-25965dup	XM_005264801.1:c.2080-25966_2080-25965dup	XM_005264801.1:c.2080-25967_2080-25965dup	XM_005264801.1:c.2080-25968_2080-25965dup	XM_005264801.1:c.2080-25969_2080-25965dup
ATG7 transcript variant X3	XM_005264802.1:c.2080-25985=	XM_005264802.1:c.2080-25977_2080-25965del	XM_005264802.1:c.2080-25976_2080-25965del	XM_005264802.1:c.2080-25973_2080-25965del	XM_005264802.1:c.2080-25972_2080-25965del	XM_005264802.1:c.2080-25971_2080-25965del	XM_005264802.1:c.2080-25970_2080-25965del	XM_005264802.1:c.2080-25969_2080-25965del	XM_005264802.1:c.2080-25968_2080-25965del	XM_005264802.1:c.2080-25967_2080-25965del	XM_005264802.1:c.2080-25966_2080-25965del	XM_005264802.1:c.2080-25965del	XM_005264802.1:c.2080-25965dup	XM_005264802.1:c.2080-25966_2080-25965dup	XM_005264802.1:c.2080-25967_2080-25965dup	XM_005264802.1:c.2080-25968_2080-25965dup	XM_005264802.1:c.2080-25969_2080-25965dup
ATG7 transcript variant X5	XM_005264804.1:c.2014-25985=	XM_005264804.1:c.2014-25977_2014-25965del	XM_005264804.1:c.2014-25976_2014-25965del	XM_005264804.1:c.2014-25973_2014-25965del	XM_005264804.1:c.2014-25972_2014-25965del	XM_005264804.1:c.2014-25971_2014-25965del	XM_005264804.1:c.2014-25970_2014-25965del	XM_005264804.1:c.2014-25969_2014-25965del	XM_005264804.1:c.2014-25968_2014-25965del	XM_005264804.1:c.2014-25967_2014-25965del	XM_005264804.1:c.2014-25966_2014-25965del	XM_005264804.1:c.2014-25965del	XM_005264804.1:c.2014-25965dup	XM_005264804.1:c.2014-25966_2014-25965dup	XM_005264804.1:c.2014-25967_2014-25965dup	XM_005264804.1:c.2014-25968_2014-25965dup	XM_005264804.1:c.2014-25969_2014-25965dup
ATG7 transcript variant X6	XM_005264805.1:c.1921-25985=	XM_005264805.1:c.1921-25977_1921-25965del	XM_005264805.1:c.1921-25976_1921-25965del	XM_005264805.1:c.1921-25973_1921-25965del	XM_005264805.1:c.1921-25972_1921-25965del	XM_005264805.1:c.1921-25971_1921-25965del	XM_005264805.1:c.1921-25970_1921-25965del	XM_005264805.1:c.1921-25969_1921-25965del	XM_005264805.1:c.1921-25968_1921-25965del	XM_005264805.1:c.1921-25967_1921-25965del	XM_005264805.1:c.1921-25966_1921-25965del	XM_005264805.1:c.1921-25965del	XM_005264805.1:c.1921-25965dup	XM_005264805.1:c.1921-25966_1921-25965dup	XM_005264805.1:c.1921-25967_1921-25965dup	XM_005264805.1:c.1921-25968_1921-25965dup	XM_005264805.1:c.1921-25969_1921-25965dup
ATG7 transcript variant X27	XM_047447308.1:c.1462-25985=	XM_047447308.1:c.1462-25977_1462-25965del	XM_047447308.1:c.1462-25976_1462-25965del	XM_047447308.1:c.1462-25973_1462-25965del	XM_047447308.1:c.1462-25972_1462-25965del	XM_047447308.1:c.1462-25971_1462-25965del	XM_047447308.1:c.1462-25970_1462-25965del	XM_047447308.1:c.1462-25969_1462-25965del	XM_047447308.1:c.1462-25968_1462-25965del	XM_047447308.1:c.1462-25967_1462-25965del	XM_047447308.1:c.1462-25966_1462-25965del	XM_047447308.1:c.1462-25965del	XM_047447308.1:c.1462-25965dup	XM_047447308.1:c.1462-25966_1462-25965dup	XM_047447308.1:c.1462-25967_1462-25965dup	XM_047447308.1:c.1462-25968_1462-25965dup	XM_047447308.1:c.1462-25969_1462-25965dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

61 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41949482	Mar 13, 2006 (126)
2	ABI	ss41952770	Mar 13, 2006 (126)
3	HGSV	ss83153432	Sep 08, 2015 (146)
4	HUMANGENOME_JCVI	ss99163139	Feb 04, 2009 (130)
5	PJP	ss295088092	May 09, 2011 (138)
6	SSMP	ss663346881	Apr 01, 2015 (144)
7	1000GENOMES	ss1369971706	Jan 10, 2018 (151)
8	EVA_UK10K_TWINSUK	ss1703512605	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1703512606	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710067341	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710067342	Apr 01, 2015 (144)
12	MCHAISSO	ss3064036603	Jan 10, 2018 (151)
13	EVA_DECODE	ss3708640072	Jul 13, 2019 (153)
14	EVA_DECODE	ss3708640073	Jul 13, 2019 (153)
15	EVA_DECODE	ss3708640074	Jul 13, 2019 (153)
16	EVA_DECODE	ss3708640075	Jul 13, 2019 (153)
17	EVA_DECODE	ss3708640076	Jul 13, 2019 (153)
18	EVA_DECODE	ss3708640077	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3802813005	Jul 13, 2019 (153)
20	EVA	ss3827662464	Apr 25, 2020 (154)
21	KOGIC	ss3950668607	Apr 25, 2020 (154)
22	KOGIC	ss3950668608	Apr 25, 2020 (154)
23	KOGIC	ss3950668609	Apr 25, 2020 (154)
24	KOGIC	ss3950668610	Apr 25, 2020 (154)
25	KOGIC	ss3950668611	Apr 25, 2020 (154)
26	GNOMAD	ss4065877913	Apr 27, 2021 (155)
27	GNOMAD	ss4065877914	Apr 27, 2021 (155)
28	GNOMAD	ss4065877915	Apr 27, 2021 (155)
29	GNOMAD	ss4065877916	Apr 27, 2021 (155)
30	GNOMAD	ss4065877917	Apr 27, 2021 (155)
31	GNOMAD	ss4065877918	Apr 27, 2021 (155)
32	GNOMAD	ss4065877919	Apr 27, 2021 (155)
33	GNOMAD	ss4065877920	Apr 27, 2021 (155)
34	GNOMAD	ss4065877921	Apr 27, 2021 (155)
35	GNOMAD	ss4065877922	Apr 27, 2021 (155)
36	GNOMAD	ss4065877923	Apr 27, 2021 (155)
37	GNOMAD	ss4065877924	Apr 27, 2021 (155)
38	GNOMAD	ss4065877925	Apr 27, 2021 (155)
39	GNOMAD	ss4065877926	Apr 27, 2021 (155)
40	TOPMED	ss4554264863	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5157805274	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5157805275	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5157805276	Apr 27, 2021 (155)
44	TOMMO_GENOMICS	ss5157805277	Apr 27, 2021 (155)
45	TOMMO_GENOMICS	ss5157805278	Apr 27, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5253054036	Oct 13, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5253054037	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5253054038	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5253054039	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5253054040	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5452554534	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5452554535	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5452554536	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5452554537	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5452554538	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5689075488	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5689075489	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5689075490	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5689075491	Oct 13, 2022 (156)
60	EVA	ss5825348054	Oct 13, 2022 (156)
61	EVA	ss5825348055	Oct 13, 2022 (156)
62	1000Genomes	NC_000003.11 - 11570300	Oct 11, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7734929 (NC_000003.11:11570300:A: 1651/3854) Row 7734930 (NC_000003.11:11570299:AAA: 354/3854)	-	Oct 11, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7734929 (NC_000003.11:11570300:A: 1651/3854) Row 7734930 (NC_000003.11:11570299:AAA: 354/3854)	-	Oct 11, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99080007 (NC_000003.12:11528825::A 14373/81070) Row 99080008 (NC_000003.12:11528825::AA 1373/81284) Row 99080009 (NC_000003.12:11528825::AAA 92/81486)...	-	Apr 27, 2021 (155)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 7046608 (NC_000003.12:11528828::A 522/1730) Row 7046609 (NC_000003.12:11528825:AAA: 17/1730) Row 7046610 (NC_000003.12:11528826:AA: 164/1730)...	-	Apr 25, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 7046608 (NC_000003.12:11528828::A 522/1730) Row 7046609 (NC_000003.12:11528825:AAA: 17/1730) Row 7046610 (NC_000003.12:11528826:AA: 164/1730)...	-	Apr 25, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 7046608 (NC_000003.12:11528828::A 522/1730) Row 7046609 (NC_000003.12:11528825:AAA: 17/1730) Row 7046610 (NC_000003.12:11528826:AA: 164/1730)...	-	Apr 25, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 7046608 (NC_000003.12:11528828::A 522/1730) Row 7046609 (NC_000003.12:11528825:AAA: 17/1730) Row 7046610 (NC_000003.12:11528826:AA: 164/1730)...	-	Apr 25, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 7046608 (NC_000003.12:11528828::A 522/1730) Row 7046609 (NC_000003.12:11528825:AAA: 17/1730) Row 7046610 (NC_000003.12:11528826:AA: 164/1730)...	-	Apr 25, 2020 (154)
84	8.3KJPN Submission ignored due to conflicting rows: Row 15774581 (NC_000003.11:11570299::A 4947/16258) Row 15774582 (NC_000003.11:11570299:AA: 1267/16258) Row 15774583 (NC_000003.11:11570299::AA 25/16258)...	-	Apr 27, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 15774581 (NC_000003.11:11570299::A 4947/16258) Row 15774582 (NC_000003.11:11570299:AA: 1267/16258) Row 15774583 (NC_000003.11:11570299::AA 25/16258)...	-	Apr 27, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 15774581 (NC_000003.11:11570299::A 4947/16258) Row 15774582 (NC_000003.11:11570299:AA: 1267/16258) Row 15774583 (NC_000003.11:11570299::AA 25/16258)...	-	Apr 27, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 15774581 (NC_000003.11:11570299::A 4947/16258) Row 15774582 (NC_000003.11:11570299:AA: 1267/16258) Row 15774583 (NC_000003.11:11570299::AA 25/16258)...	-	Apr 27, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 15774581 (NC_000003.11:11570299::A 4947/16258) Row 15774582 (NC_000003.11:11570299:AA: 1267/16258) Row 15774583 (NC_000003.11:11570299::AA 25/16258)...	-	Apr 27, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 22912592 (NC_000003.12:11528825::A 8081/27266) Row 22912593 (NC_000003.12:11528825:AA: 2267/27266) Row 22912594 (NC_000003.12:11528825::AA 45/27266)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 22912592 (NC_000003.12:11528825::A 8081/27266) Row 22912593 (NC_000003.12:11528825:AA: 2267/27266) Row 22912594 (NC_000003.12:11528825::AA 45/27266)...	-	Oct 13, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 22912592 (NC_000003.12:11528825::A 8081/27266) Row 22912593 (NC_000003.12:11528825:AA: 2267/27266) Row 22912594 (NC_000003.12:11528825::AA 45/27266)...	-	Oct 13, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 22912592 (NC_000003.12:11528825::A 8081/27266) Row 22912593 (NC_000003.12:11528825:AA: 2267/27266) Row 22912594 (NC_000003.12:11528825::AA 45/27266)...	-	Oct 13, 2022 (156)
93	TopMed	NC_000003.12 - 11528826	Apr 27, 2021 (155)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7734929 (NC_000003.11:11570300:A: 1568/3708) Row 7734930 (NC_000003.11:11570299:AAA: 354/3708)	-	Oct 11, 2018 (152)
95	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7734929 (NC_000003.11:11570300:A: 1568/3708) Row 7734930 (NC_000003.11:11570299:AAA: 354/3708)	-	Oct 11, 2018 (152)
96	ALFA	NC_000003.12 - 11528826	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs34760206	May 15, 2013 (138)
rs57129840	May 11, 2012 (137)
rs72072243	May 11, 2012 (137)
rs144808192	May 11, 2012 (137)
rs562739593	Apr 01, 2015 (144)
rs796777633	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
391642418, ss4554264863	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4065877926	NC_000003.12:11528825:AAAAAAAAAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4065877925	NC_000003.12:11528825:AAAAAAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5157805278	NC_000003.11:11570299:AAAAAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4065877924	NC_000003.12:11528825:AAAAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4065877923	NC_000003.12:11528825:AAAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4065877922	NC_000003.12:11528825:AAAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3708640077, ss4065877921	NC_000003.12:11528825:AAAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1703512605, ss1703512606, ss5825348055	NC_000003.11:11570299:AAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3950668608, ss4065877920, ss5253054040, ss5452554538	NC_000003.12:11528825:AAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3708640076	NC_000003.12:11528826:AAA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss83153432	NC_000003.9:11545318:AA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
13954605, ss1369971706, ss5157805275, ss5825348054	NC_000003.11:11570299:AA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1710067341, ss1710067342	NC_000003.11:11570300:AA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3802813005, ss4065877919, ss5253054037, ss5452554535, ss5689075489	NC_000003.12:11528825:AA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3950668609	NC_000003.12:11528826:AA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3708640075	NC_000003.12:11528827:AA:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5157805277	NC_000003.11:11570299:A:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
	NC_000003.11:11570300:A:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4065877918, ss5253054038, ss5452554534, ss5689075491	NC_000003.12:11528825:A:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3950668611	NC_000003.12:11528827:A:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3708640074	NC_000003.12:11528828:A:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss41949482	NT_022517.18:11510299:A:	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss295088092	NC_000003.10:11545320::A	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss663346881, ss3827662464, ss5157805274	NC_000003.11:11570299::A	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3064036603, ss4065877913, ss5253054036, ss5452554536, ss5689075488	NC_000003.12:11528825::A	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3950668607	NC_000003.12:11528828::A	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3708640073	NC_000003.12:11528829::A	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss41952770, ss99163139	NT_022517.18:11510299::A	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5157805276	NC_000003.11:11570299::AA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4065877914, ss5253054039, ss5452554537, ss5689075490	NC_000003.12:11528825::AA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3950668610	NC_000003.12:11528828::AA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3708640072	NC_000003.12:11528829::AA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4065877915	NC_000003.12:11528825::AAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
7513414041	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4065877916	NC_000003.12:11528825::AAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4065877917	NC_000003.12:11528825::AAAAA	NC_000003.12:11528825:AAAAAAAAAAAA… NC_000003.12:11528825:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs11377789

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11377789