Name: rs554471580
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.

rs554471580

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:179929951-179929972 (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)₁₁ / d…
del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₅ / dup(A)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.00000 (0/10822, ALFA)
del(A)₁₂=0.00000 (0/10822, ALFA)
del(A)₁₁=0.00000 (0/10822, ALFA) (+ 12 more)
del(A)₁₀=0.00000 (0/10822, ALFA)
del(A)₉=0.00000 (0/10822, ALFA)
del(A)₈=0.00000 (0/10822, ALFA)
del(A)₇=0.00000 (0/10822, ALFA)
del(A)₆=0.00000 (0/10822, ALFA)
del(A)₄=0.00000 (0/10822, ALFA)
delAAA=0.00000 (0/10822, ALFA)
delAA=0.00000 (0/10822, ALFA)
delA=0.00000 (0/10822, ALFA)
dupA=0.00000 (0/10822, ALFA)
dupAA=0.00000 (0/10822, ALFA)
dupAAA=0.00000 (0/10822, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC101928933 : 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	10822	AAAAAAAAAAAAAAAAAAAAAA=1.00000	AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	7368	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2136	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	76	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	2060	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	106	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
East Asian	Sub	84	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	138	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	572	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	88	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	414	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	10822	(A)₂₂=1.00000	del(A)₁₃=0.00000, del(A)₁₂=0.00000, del(A)₁₁=0.00000, del(A)₁₀=0.00000, del(A)₉=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₆=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000, dupAAA=0.00000
Allele Frequency Aggregator	European	Sub	7368	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=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	2136	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=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	Latin American 2	Sub	572	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=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	414	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=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 1	Sub	138	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=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	106	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=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	South Asian	Sub	88	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=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

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 1	NC_000001.11:g.179929960_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929961_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929962_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929963_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929964_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929965_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929966_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929967_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929969_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929970_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929971_179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929972del
GRCh38.p14 chr 1	NC_000001.11:g.179929972dup
GRCh38.p14 chr 1	NC_000001.11:g.179929971_179929972dup
GRCh38.p14 chr 1	NC_000001.11:g.179929970_179929972dup
GRCh38.p14 chr 1	NC_000001.11:g.179929968_179929972dup
GRCh38.p14 chr 1	NC_000001.11:g.179929960_179929972dup
GRCh37.p13 chr 1	NC_000001.10:g.179899095_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899096_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899097_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899098_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899099_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899100_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899101_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899102_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899104_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899105_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899106_179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899107del
GRCh37.p13 chr 1	NC_000001.10:g.179899107dup
GRCh37.p13 chr 1	NC_000001.10:g.179899106_179899107dup
GRCh37.p13 chr 1	NC_000001.10:g.179899105_179899107dup
GRCh37.p13 chr 1	NC_000001.10:g.179899103_179899107dup
GRCh37.p13 chr 1	NC_000001.10:g.179899095_179899107dup

Gene: LOC101928933, uncharacterized LOC101928933 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC101928933 transcript variant X1	XR_241158.4: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)₂₂=	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₅	dup(A)₁₃
GRCh38.p14 chr 1	NC_000001.11:g.179929951_179929972=	NC_000001.11:g.179929960_179929972del	NC_000001.11:g.179929961_179929972del	NC_000001.11:g.179929962_179929972del	NC_000001.11:g.179929963_179929972del	NC_000001.11:g.179929964_179929972del	NC_000001.11:g.179929965_179929972del	NC_000001.11:g.179929966_179929972del	NC_000001.11:g.179929967_179929972del	NC_000001.11:g.179929969_179929972del	NC_000001.11:g.179929970_179929972del	NC_000001.11:g.179929971_179929972del	NC_000001.11:g.179929972del	NC_000001.11:g.179929972dup	NC_000001.11:g.179929971_179929972dup	NC_000001.11:g.179929970_179929972dup	NC_000001.11:g.179929968_179929972dup	NC_000001.11:g.179929960_179929972dup
GRCh37.p13 chr 1	NC_000001.10:g.179899086_179899107=	NC_000001.10:g.179899095_179899107del	NC_000001.10:g.179899096_179899107del	NC_000001.10:g.179899097_179899107del	NC_000001.10:g.179899098_179899107del	NC_000001.10:g.179899099_179899107del	NC_000001.10:g.179899100_179899107del	NC_000001.10:g.179899101_179899107del	NC_000001.10:g.179899102_179899107del	NC_000001.10:g.179899104_179899107del	NC_000001.10:g.179899105_179899107del	NC_000001.10:g.179899106_179899107del	NC_000001.10:g.179899107del	NC_000001.10:g.179899107dup	NC_000001.10:g.179899106_179899107dup	NC_000001.10:g.179899105_179899107dup	NC_000001.10:g.179899103_179899107dup	NC_000001.10:g.179899095_179899107dup

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#.

43 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSIP	ss947034400	Aug 21, 2014 (142)
2	EVA	ss3826515356	Apr 25, 2020 (154)
3	KOGIC	ss3945998093	Apr 25, 2020 (154)
4	KOGIC	ss3945998094	Apr 25, 2020 (154)
5	KOGIC	ss3945998095	Apr 25, 2020 (154)
6	KOGIC	ss3945998096	Apr 25, 2020 (154)
7	KOGIC	ss3945998097	Apr 25, 2020 (154)
8	GNOMAD	ss4006765146	Apr 25, 2021 (155)
9	GNOMAD	ss4006765147	Apr 25, 2021 (155)
10	GNOMAD	ss4006765148	Apr 25, 2021 (155)
11	GNOMAD	ss4006765149	Apr 25, 2021 (155)
12	GNOMAD	ss4006765150	Apr 25, 2021 (155)
13	GNOMAD	ss4006765151	Apr 25, 2021 (155)
14	GNOMAD	ss4006765152	Apr 25, 2021 (155)
15	GNOMAD	ss4006765153	Apr 25, 2021 (155)
16	GNOMAD	ss4006765154	Apr 25, 2021 (155)
17	GNOMAD	ss4006765155	Apr 25, 2021 (155)
18	GNOMAD	ss4006765156	Apr 25, 2021 (155)
19	GNOMAD	ss4006765157	Apr 25, 2021 (155)
20	GNOMAD	ss4006765158	Apr 25, 2021 (155)
21	TOPMED	ss4474493989	Apr 25, 2021 (155)
22	TOPMED	ss4474493990	Apr 25, 2021 (155)
23	TOPMED	ss4474493991	Apr 25, 2021 (155)
24	TOPMED	ss4474493992	Apr 25, 2021 (155)
25	TOPMED	ss4474493993	Apr 25, 2021 (155)
26	TOMMO_GENOMICS	ss5147275103	Apr 25, 2021 (155)
27	TOMMO_GENOMICS	ss5147275104	Apr 25, 2021 (155)
28	TOMMO_GENOMICS	ss5147275105	Apr 25, 2021 (155)
29	TOMMO_GENOMICS	ss5147275106	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5147275107	Apr 25, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5244900390	Oct 17, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5244900391	Oct 17, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5244900392	Oct 17, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5244900393	Oct 17, 2022 (156)
35	HUGCELL_USP	ss5445425127	Oct 17, 2022 (156)
36	HUGCELL_USP	ss5445425128	Oct 17, 2022 (156)
37	HUGCELL_USP	ss5445425129	Oct 17, 2022 (156)
38	HUGCELL_USP	ss5445425130	Oct 17, 2022 (156)
39	TOMMO_GENOMICS	ss5674702460	Oct 17, 2022 (156)
40	TOMMO_GENOMICS	ss5674702461	Oct 17, 2022 (156)
41	TOMMO_GENOMICS	ss5674702462	Oct 17, 2022 (156)
42	TOMMO_GENOMICS	ss5674702463	Oct 17, 2022 (156)
43	TOMMO_GENOMICS	ss5674702465	Oct 17, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32112600 (NC_000001.11:179929950::A 1892/40580) Row 32112601 (NC_000001.11:179929950::AA 183/42104) Row 32112602 (NC_000001.11:179929950::AAA 13/43216)...	-	Apr 25, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 2376094 (NC_000001.11:179929952:A: 206/1702) Row 2376095 (NC_000001.11:179929953::A 248/1702) Row 2376096 (NC_000001.11:179929953::AA 39/1702)...	-	Apr 25, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 2376094 (NC_000001.11:179929952:A: 206/1702) Row 2376095 (NC_000001.11:179929953::A 248/1702) Row 2376096 (NC_000001.11:179929953::AA 39/1702)...	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 2376094 (NC_000001.11:179929952:A: 206/1702) Row 2376095 (NC_000001.11:179929953::A 248/1702) Row 2376096 (NC_000001.11:179929953::AA 39/1702)...	-	Apr 25, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 2376094 (NC_000001.11:179929952:A: 206/1702) Row 2376095 (NC_000001.11:179929953::A 248/1702) Row 2376096 (NC_000001.11:179929953::AA 39/1702)...	-	Apr 25, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 2376094 (NC_000001.11:179929952:A: 206/1702) Row 2376095 (NC_000001.11:179929953::A 248/1702) Row 2376096 (NC_000001.11:179929953::AA 39/1702)...	-	Apr 25, 2020 (154)
63	8.3KJPN Submission ignored due to conflicting rows: Row 5244410 (NC_000001.10:179899085:A: 151/16740) Row 5244411 (NC_000001.10:179899085::A 101/16740) Row 5244412 (NC_000001.10:179899085:AAAAAAAAAAA: 6/16740)...	-	Apr 25, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 5244410 (NC_000001.10:179899085:A: 151/16740) Row 5244411 (NC_000001.10:179899085::A 101/16740) Row 5244412 (NC_000001.10:179899085:AAAAAAAAAAA: 6/16740)...	-	Apr 25, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 5244410 (NC_000001.10:179899085:A: 151/16740) Row 5244411 (NC_000001.10:179899085::A 101/16740) Row 5244412 (NC_000001.10:179899085:AAAAAAAAAAA: 6/16740)...	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 5244410 (NC_000001.10:179899085:A: 151/16740) Row 5244411 (NC_000001.10:179899085::A 101/16740) Row 5244412 (NC_000001.10:179899085:AAAAAAAAAAA: 6/16740)...	-	Apr 25, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 5244410 (NC_000001.10:179899085:A: 151/16740) Row 5244411 (NC_000001.10:179899085::A 101/16740) Row 5244412 (NC_000001.10:179899085:AAAAAAAAAAA: 6/16740)...	-	Apr 25, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 8539564 (NC_000001.11:179929950:A: 291/28200) Row 8539565 (NC_000001.11:179929950::A 149/28200) Row 8539566 (NC_000001.11:179929950:AAAAAAAAAAA: 11/28200)...	-	Oct 17, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 8539564 (NC_000001.11:179929950:A: 291/28200) Row 8539565 (NC_000001.11:179929950::A 149/28200) Row 8539566 (NC_000001.11:179929950:AAAAAAAAAAA: 11/28200)...	-	Oct 17, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 8539564 (NC_000001.11:179929950:A: 291/28200) Row 8539565 (NC_000001.11:179929950::A 149/28200) Row 8539566 (NC_000001.11:179929950:AAAAAAAAAAA: 11/28200)...	-	Oct 17, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 8539564 (NC_000001.11:179929950:A: 291/28200) Row 8539565 (NC_000001.11:179929950::A 149/28200) Row 8539566 (NC_000001.11:179929950:AAAAAAAAAAA: 11/28200)...	-	Oct 17, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 8539564 (NC_000001.11:179929950:A: 291/28200) Row 8539565 (NC_000001.11:179929950::A 149/28200) Row 8539566 (NC_000001.11:179929950:AAAAAAAAAAA: 11/28200)...	-	Oct 17, 2022 (156)
73	TopMed Submission ignored due to conflicting rows: Row 38100324 (NC_000001.11:179929950:AAAAAAAA: 165/264690) Row 38100325 (NC_000001.11:179929950:AAAAAAAAAA: 1/264690) Row 38100326 (NC_000001.11:179929950:AAAAAAAAAAA: 3/264690)...	-	Apr 25, 2021 (155)
74	TopMed Submission ignored due to conflicting rows: Row 38100324 (NC_000001.11:179929950:AAAAAAAA: 165/264690) Row 38100325 (NC_000001.11:179929950:AAAAAAAAAA: 1/264690) Row 38100326 (NC_000001.11:179929950:AAAAAAAAAAA: 3/264690)...	-	Apr 25, 2021 (155)
75	TopMed Submission ignored due to conflicting rows: Row 38100324 (NC_000001.11:179929950:AAAAAAAA: 165/264690) Row 38100325 (NC_000001.11:179929950:AAAAAAAAAA: 1/264690) Row 38100326 (NC_000001.11:179929950:AAAAAAAAAAA: 3/264690)...	-	Apr 25, 2021 (155)
76	TopMed Submission ignored due to conflicting rows: Row 38100324 (NC_000001.11:179929950:AAAAAAAA: 165/264690) Row 38100325 (NC_000001.11:179929950:AAAAAAAAAA: 1/264690) Row 38100326 (NC_000001.11:179929950:AAAAAAAAAAA: 3/264690)...	-	Apr 25, 2021 (155)
77	TopMed Submission ignored due to conflicting rows: Row 38100324 (NC_000001.11:179929950:AAAAAAAA: 165/264690) Row 38100325 (NC_000001.11:179929950:AAAAAAAAAA: 1/264690) Row 38100326 (NC_000001.11:179929950:AAAAAAAAAAA: 3/264690)...	-	Apr 25, 2021 (155)
78	ALFA	NC_000001.11 - 179929951	Apr 25, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4006765158, ss4474493993	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4006765157, ss4474493992	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5147275105	NC_000001.10:179899085:AAAAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4006765156, ss4474493991, ss5674702462	NC_000001.11:179929950:AAAAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4474493990	NC_000001.11:179929950:AAAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4006765155, ss4474493989	NC_000001.11:179929950:AAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5147275106	NC_000001.10:179899085:AAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4006765154, ss5674702463	NC_000001.11:179929950:AAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4006765153	NC_000001.11:179929950:AAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4006765152	NC_000001.11:179929950:AAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3945998097	NC_000001.11:179929950:AAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5147275107	NC_000001.10:179899085:AA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4006765151, ss5244900393, ss5445425130, ss5674702465	NC_000001.11:179929950:AA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3945998096	NC_000001.11:179929951:AA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5147275103	NC_000001.10:179899085:A:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5244900391, ss5445425129, ss5674702460	NC_000001.11:179929950:A:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3945998093	NC_000001.11:179929952:A:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3826515356, ss5147275104	NC_000001.10:179899085::A	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss947034400	NC_000001.10:179899086::A	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4006765146, ss5244900390, ss5445425127, ss5674702461	NC_000001.11:179929950::A	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3945998094	NC_000001.11:179929953::A	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4006765147, ss5244900392, ss5445425128	NC_000001.11:179929950::AA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3945998095	NC_000001.11:179929953::AA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4006765148	NC_000001.11:179929950::AAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10344476328	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4006765149	NC_000001.11:179929950::AAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4006765150	NC_000001.11:179929950::AAAAAAAAAA… NC_000001.11:179929950::AAAAAAAAAAAAA	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2330525617	NC_000001.10:179899085:AAAAAAAAAAA… NC_000001.10:179899085:AAAAAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA
ss3096701554	NC_000001.11:179929950:AAAAAAAAA:	NC_000001.11:179929950:AAAAAAAAAAA… NC_000001.11:179929950:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

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

No publications for rs554471580

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

rs554471580