Name: rs11300466
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.

rs11300466

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:101116740-101116762 (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)₅ / delAAA / delA…
del(A)₁₃ / del(A)₅ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₁₁ / dup(A)₁₂ / dup(A)₁₈ / dup(A)₂₁ / ins(A)₃₆ / ins(A)₄₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.0000 (0/3504, ALFA)
del(A)₅=0.0000 (0/3504, ALFA)
delAAA=0.0000 (0/3504, ALFA) (+ 4 more)
delAA=0.0000 (0/3504, ALFA)
delA=0.0000 (0/3504, ALFA)
dupA=0.0000 (0/3504, ALFA)
dupAA=0.0000 (0/3504, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PGR : 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	3504	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1940	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1036	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	50	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	986	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	56	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	44	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	46	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	208	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	42	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	176	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=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	3504	(A)₂₃=1.0000	del(A)₁₃=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	1940	(A)₂₃=1.0000	del(A)₁₃=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	1036	(A)₂₃=1.0000	del(A)₁₃=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	208	(A)₂₃=1.000	del(A)₁₃=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	176	(A)₂₃=1.000	del(A)₁₃=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	56	(A)₂₃=1.00	del(A)₁₃=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	46	(A)₂₃=1.00	del(A)₁₃=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(A)₂₃=1.00	del(A)₁₃=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=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 11	NC_000011.10:g.101116750_101116762del
GRCh38.p14 chr 11	NC_000011.10:g.101116758_101116762del
GRCh38.p14 chr 11	NC_000011.10:g.101116760_101116762del
GRCh38.p14 chr 11	NC_000011.10:g.101116761_101116762del
GRCh38.p14 chr 11	NC_000011.10:g.101116762del
GRCh38.p14 chr 11	NC_000011.10:g.101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116761_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116760_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116759_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116758_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116757_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116756_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116752_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116751_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116745_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116742_101116762dup
GRCh38.p14 chr 11	NC_000011.10:g.101116762_101116763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 11	NC_000011.10:g.101116762_101116763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.100987481_100987493del
GRCh37.p13 chr 11	NC_000011.9:g.100987489_100987493del
GRCh37.p13 chr 11	NC_000011.9:g.100987491_100987493del
GRCh37.p13 chr 11	NC_000011.9:g.100987492_100987493del
GRCh37.p13 chr 11	NC_000011.9:g.100987493del
GRCh37.p13 chr 11	NC_000011.9:g.100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987492_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987491_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987490_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987489_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987488_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987487_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987483_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987482_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987476_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987473_100987493dup
GRCh37.p13 chr 11	NC_000011.9:g.100987493_100987494insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.100987493_100987494insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
PGR RefSeqGene	NG_016475.1:g.18062_18074del
PGR RefSeqGene	NG_016475.1:g.18070_18074del
PGR RefSeqGene	NG_016475.1:g.18072_18074del
PGR RefSeqGene	NG_016475.1:g.18073_18074del
PGR RefSeqGene	NG_016475.1:g.18074del
PGR RefSeqGene	NG_016475.1:g.18074dup
PGR RefSeqGene	NG_016475.1:g.18073_18074dup
PGR RefSeqGene	NG_016475.1:g.18072_18074dup
PGR RefSeqGene	NG_016475.1:g.18071_18074dup
PGR RefSeqGene	NG_016475.1:g.18070_18074dup
PGR RefSeqGene	NG_016475.1:g.18069_18074dup
PGR RefSeqGene	NG_016475.1:g.18068_18074dup
PGR RefSeqGene	NG_016475.1:g.18064_18074dup
PGR RefSeqGene	NG_016475.1:g.18063_18074dup
PGR RefSeqGene	NG_016475.1:g.18057_18074dup
PGR RefSeqGene	NG_016475.1:g.18054_18074dup
PGR RefSeqGene	NG_016475.1:g.18074_18075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR RefSeqGene	NG_016475.1:g.18074_18075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: PGR, progesterone receptor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PGR transcript variant 2	NM_000926.4:c.1789+9255_1… NM_000926.4:c.1789+9255_1789+9267del	N/A	Intron Variant
PGR transcript variant 1	NM_001202474.3:c.1297+925… NM_001202474.3:c.1297+9255_1297+9267del	N/A	Intron Variant
PGR transcript variant 3	NM_001271161.2:c.1297+925… NM_001271161.2:c.1297+9255_1297+9267del	N/A	Intron Variant
PGR transcript variant 7	NM_001271162.2:c.7+9255_7… NM_001271162.2:c.7+9255_7+9267del	N/A	Intron Variant
PGR transcript variant 4	NR_073141.3:n.	N/A	Intron Variant
PGR transcript variant 5	NR_073142.3:n.	N/A	Intron Variant
PGR transcript variant 6	NR_073143.3:n.	N/A	Intron Variant
PGR transcript variant X1	XM_006718858.4:c.1789+925… XM_006718858.4:c.1789+9255_1789+9267del	N/A	Intron Variant
PGR transcript variant X2	XM_011542869.3:c.3510_3… XM_011542869.3:c.3510_3532=	N/A	3 Prime UTR 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)₂₃=	del(A)₁₃	del(A)₅	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₁₁	dup(A)₁₂	dup(A)₁₈	dup(A)₂₁	ins(A)₃₆	ins(A)₄₀
GRCh38.p14 chr 11	NC_000011.10:g.101116740_101116762=	NC_000011.10:g.101116750_101116762del	NC_000011.10:g.101116758_101116762del	NC_000011.10:g.101116760_101116762del	NC_000011.10:g.101116761_101116762del	NC_000011.10:g.101116762del	NC_000011.10:g.101116762dup	NC_000011.10:g.101116761_101116762dup	NC_000011.10:g.101116760_101116762dup	NC_000011.10:g.101116759_101116762dup	NC_000011.10:g.101116758_101116762dup	NC_000011.10:g.101116757_101116762dup	NC_000011.10:g.101116756_101116762dup	NC_000011.10:g.101116752_101116762dup	NC_000011.10:g.101116751_101116762dup	NC_000011.10:g.101116745_101116762dup	NC_000011.10:g.101116742_101116762dup	NC_000011.10:g.101116762_101116763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:g.101116762_101116763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.100987471_100987493=	NC_000011.9:g.100987481_100987493del	NC_000011.9:g.100987489_100987493del	NC_000011.9:g.100987491_100987493del	NC_000011.9:g.100987492_100987493del	NC_000011.9:g.100987493del	NC_000011.9:g.100987493dup	NC_000011.9:g.100987492_100987493dup	NC_000011.9:g.100987491_100987493dup	NC_000011.9:g.100987490_100987493dup	NC_000011.9:g.100987489_100987493dup	NC_000011.9:g.100987488_100987493dup	NC_000011.9:g.100987487_100987493dup	NC_000011.9:g.100987483_100987493dup	NC_000011.9:g.100987482_100987493dup	NC_000011.9:g.100987476_100987493dup	NC_000011.9:g.100987473_100987493dup	NC_000011.9:g.100987493_100987494insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.9:g.100987493_100987494insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
PGR RefSeqGene	NG_016475.1:g.18052_18074=	NG_016475.1:g.18062_18074del	NG_016475.1:g.18070_18074del	NG_016475.1:g.18072_18074del	NG_016475.1:g.18073_18074del	NG_016475.1:g.18074del	NG_016475.1:g.18074dup	NG_016475.1:g.18073_18074dup	NG_016475.1:g.18072_18074dup	NG_016475.1:g.18071_18074dup	NG_016475.1:g.18070_18074dup	NG_016475.1:g.18069_18074dup	NG_016475.1:g.18068_18074dup	NG_016475.1:g.18064_18074dup	NG_016475.1:g.18063_18074dup	NG_016475.1:g.18057_18074dup	NG_016475.1:g.18054_18074dup	NG_016475.1:g.18074_18075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NG_016475.1:g.18074_18075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant X2	XM_011542869.3:c.3510_3532=	XM_011542869.3:c.3520_3532del	XM_011542869.3:c.3528_3532del	XM_011542869.3:c.3530_3532del	XM_011542869.3:c.3531_3532del	XM_011542869.3:c.*3532del	XM_011542869.3:c.*3532dup	XM_011542869.3:c.3531_3532dup	XM_011542869.3:c.3530_3532dup	XM_011542869.3:c.3529_3532dup	XM_011542869.3:c.3528_3532dup	XM_011542869.3:c.3527_3532dup	XM_011542869.3:c.3526_3532dup	XM_011542869.3:c.3522_3532dup	XM_011542869.3:c.3521_3532dup	XM_011542869.3:c.3515_3532dup	XM_011542869.3:c.3512_3532dup	XM_011542869.3:c.3532_3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011542869.3:c.3532_3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant X2	XM_011542869.2:c.3510_3532=	XM_011542869.2:c.3520_3532del	XM_011542869.2:c.3528_3532del	XM_011542869.2:c.3530_3532del	XM_011542869.2:c.3531_3532del	XM_011542869.2:c.*3532del	XM_011542869.2:c.*3532dup	XM_011542869.2:c.3531_3532dup	XM_011542869.2:c.3530_3532dup	XM_011542869.2:c.3529_3532dup	XM_011542869.2:c.3528_3532dup	XM_011542869.2:c.3527_3532dup	XM_011542869.2:c.3526_3532dup	XM_011542869.2:c.3522_3532dup	XM_011542869.2:c.3521_3532dup	XM_011542869.2:c.3515_3532dup	XM_011542869.2:c.3512_3532dup	XM_011542869.2:c.3532_3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011542869.2:c.3532_3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant 2	NM_000926.4:c.1789+9267=	NM_000926.4:c.1789+9255_1789+9267del	NM_000926.4:c.1789+9263_1789+9267del	NM_000926.4:c.1789+9265_1789+9267del	NM_000926.4:c.1789+9266_1789+9267del	NM_000926.4:c.1789+9267del	NM_000926.4:c.1789+9267dup	NM_000926.4:c.1789+9266_1789+9267dup	NM_000926.4:c.1789+9265_1789+9267dup	NM_000926.4:c.1789+9264_1789+9267dup	NM_000926.4:c.1789+9263_1789+9267dup	NM_000926.4:c.1789+9262_1789+9267dup	NM_000926.4:c.1789+9261_1789+9267dup	NM_000926.4:c.1789+9257_1789+9267dup	NM_000926.4:c.1789+9256_1789+9267dup	NM_000926.4:c.1789+9250_1789+9267dup	NM_000926.4:c.1789+9247_1789+9267dup	NM_000926.4:c.1789+9267_1789+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_000926.4:c.1789+9267_1789+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant 1	NM_001202474.3:c.1297+9267=	NM_001202474.3:c.1297+9255_1297+9267del	NM_001202474.3:c.1297+9263_1297+9267del	NM_001202474.3:c.1297+9265_1297+9267del	NM_001202474.3:c.1297+9266_1297+9267del	NM_001202474.3:c.1297+9267del	NM_001202474.3:c.1297+9267dup	NM_001202474.3:c.1297+9266_1297+9267dup	NM_001202474.3:c.1297+9265_1297+9267dup	NM_001202474.3:c.1297+9264_1297+9267dup	NM_001202474.3:c.1297+9263_1297+9267dup	NM_001202474.3:c.1297+9262_1297+9267dup	NM_001202474.3:c.1297+9261_1297+9267dup	NM_001202474.3:c.1297+9257_1297+9267dup	NM_001202474.3:c.1297+9256_1297+9267dup	NM_001202474.3:c.1297+9250_1297+9267dup	NM_001202474.3:c.1297+9247_1297+9267dup	NM_001202474.3:c.1297+9267_1297+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001202474.3:c.1297+9267_1297+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant 3	NM_001271161.2:c.1297+9267=	NM_001271161.2:c.1297+9255_1297+9267del	NM_001271161.2:c.1297+9263_1297+9267del	NM_001271161.2:c.1297+9265_1297+9267del	NM_001271161.2:c.1297+9266_1297+9267del	NM_001271161.2:c.1297+9267del	NM_001271161.2:c.1297+9267dup	NM_001271161.2:c.1297+9266_1297+9267dup	NM_001271161.2:c.1297+9265_1297+9267dup	NM_001271161.2:c.1297+9264_1297+9267dup	NM_001271161.2:c.1297+9263_1297+9267dup	NM_001271161.2:c.1297+9262_1297+9267dup	NM_001271161.2:c.1297+9261_1297+9267dup	NM_001271161.2:c.1297+9257_1297+9267dup	NM_001271161.2:c.1297+9256_1297+9267dup	NM_001271161.2:c.1297+9250_1297+9267dup	NM_001271161.2:c.1297+9247_1297+9267dup	NM_001271161.2:c.1297+9267_1297+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001271161.2:c.1297+9267_1297+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant 7	NM_001271162.1:c.7+9267=	NM_001271162.1:c.7+9255_7+9267del	NM_001271162.1:c.7+9263_7+9267del	NM_001271162.1:c.7+9265_7+9267del	NM_001271162.1:c.7+9266_7+9267del	NM_001271162.1:c.7+9267del	NM_001271162.1:c.7+9267dup	NM_001271162.1:c.7+9266_7+9267dup	NM_001271162.1:c.7+9265_7+9267dup	NM_001271162.1:c.7+9264_7+9267dup	NM_001271162.1:c.7+9263_7+9267dup	NM_001271162.1:c.7+9262_7+9267dup	NM_001271162.1:c.7+9261_7+9267dup	NM_001271162.1:c.7+9257_7+9267dup	NM_001271162.1:c.7+9256_7+9267dup	NM_001271162.1:c.7+9250_7+9267dup	NM_001271162.1:c.7+9247_7+9267dup	NM_001271162.1:c.7+9267_7+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001271162.1:c.7+9267_7+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant 7	NM_001271162.2:c.7+9267=	NM_001271162.2:c.7+9255_7+9267del	NM_001271162.2:c.7+9263_7+9267del	NM_001271162.2:c.7+9265_7+9267del	NM_001271162.2:c.7+9266_7+9267del	NM_001271162.2:c.7+9267del	NM_001271162.2:c.7+9267dup	NM_001271162.2:c.7+9266_7+9267dup	NM_001271162.2:c.7+9265_7+9267dup	NM_001271162.2:c.7+9264_7+9267dup	NM_001271162.2:c.7+9263_7+9267dup	NM_001271162.2:c.7+9262_7+9267dup	NM_001271162.2:c.7+9261_7+9267dup	NM_001271162.2:c.7+9257_7+9267dup	NM_001271162.2:c.7+9256_7+9267dup	NM_001271162.2:c.7+9250_7+9267dup	NM_001271162.2:c.7+9247_7+9267dup	NM_001271162.2:c.7+9267_7+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001271162.2:c.7+9267_7+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PGR transcript variant X1	XM_006718858.4:c.1789+9267=	XM_006718858.4:c.1789+9255_1789+9267del	XM_006718858.4:c.1789+9263_1789+9267del	XM_006718858.4:c.1789+9265_1789+9267del	XM_006718858.4:c.1789+9266_1789+9267del	XM_006718858.4:c.1789+9267del	XM_006718858.4:c.1789+9267dup	XM_006718858.4:c.1789+9266_1789+9267dup	XM_006718858.4:c.1789+9265_1789+9267dup	XM_006718858.4:c.1789+9264_1789+9267dup	XM_006718858.4:c.1789+9263_1789+9267dup	XM_006718858.4:c.1789+9262_1789+9267dup	XM_006718858.4:c.1789+9261_1789+9267dup	XM_006718858.4:c.1789+9257_1789+9267dup	XM_006718858.4:c.1789+9256_1789+9267dup	XM_006718858.4:c.1789+9250_1789+9267dup	XM_006718858.4:c.1789+9247_1789+9267dup	XM_006718858.4:c.1789+9267_1789+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_006718858.4:c.1789+9267_1789+9268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

35 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294719160	May 09, 2011 (137)
2	SWEGEN	ss3008665726	Nov 08, 2017 (151)
3	PACBIO	ss3792175095	Jul 13, 2019 (153)
4	EVA	ss3832802918	Apr 26, 2020 (154)
5	GNOMAD	ss4241245973	Apr 26, 2021 (155)
6	GNOMAD	ss4241245974	Apr 26, 2021 (155)
7	GNOMAD	ss4241245975	Apr 26, 2021 (155)
8	GNOMAD	ss4241245976	Apr 26, 2021 (155)
9	GNOMAD	ss4241245977	Apr 26, 2021 (155)
10	GNOMAD	ss4241245978	Apr 26, 2021 (155)
11	GNOMAD	ss4241245979	Apr 26, 2021 (155)
12	GNOMAD	ss4241245980	Apr 26, 2021 (155)
13	GNOMAD	ss4241245981	Apr 26, 2021 (155)
14	GNOMAD	ss4241245982	Apr 26, 2021 (155)
15	GNOMAD	ss4241245983	Apr 26, 2021 (155)
16	GNOMAD	ss4241245984	Apr 26, 2021 (155)
17	GNOMAD	ss4241245985	Apr 26, 2021 (155)
18	GNOMAD	ss4241245987	Apr 26, 2021 (155)
19	GNOMAD	ss4241245988	Apr 26, 2021 (155)
20	GNOMAD	ss4241245989	Apr 26, 2021 (155)
21	GNOMAD	ss4241245990	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5203571721	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5203571722	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5203571723	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5288653656	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5288653657	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5288653658	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5483667551	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5483667552	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5483667553	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5483667554	Oct 16, 2022 (156)
32	SANFORD_IMAGENETICS	ss5651931093	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5751928424	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5751928425	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5751928426	Oct 16, 2022 (156)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 389878449 (NC_000011.10:101116739::A 4041/63730) Row 389878450 (NC_000011.10:101116739::AA 359/63476) Row 389878451 (NC_000011.10:101116739::AAA 48/64188)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 61541028 (NC_000011.9:100987470:A: 1857/16716) Row 61541029 (NC_000011.9:100987470::A 70/16716) Row 61541030 (NC_000011.9:100987470:AA: 4/16716)	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 61541028 (NC_000011.9:100987470:A: 1857/16716) Row 61541029 (NC_000011.9:100987470::A 70/16716) Row 61541030 (NC_000011.9:100987470:AA: 4/16716)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 61541028 (NC_000011.9:100987470:A: 1857/16716) Row 61541029 (NC_000011.9:100987470::A 70/16716) Row 61541030 (NC_000011.9:100987470:AA: 4/16716)	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 85765528 (NC_000011.10:101116739:A: 3991/28206) Row 85765529 (NC_000011.10:101116739::A 86/28206) Row 85765530 (NC_000011.10:101116739:AA: 8/28206)	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 85765528 (NC_000011.10:101116739:A: 3991/28206) Row 85765529 (NC_000011.10:101116739::A 86/28206) Row 85765530 (NC_000011.10:101116739:AA: 8/28206)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 85765528 (NC_000011.10:101116739:A: 3991/28206) Row 85765529 (NC_000011.10:101116739::A 86/28206) Row 85765530 (NC_000011.10:101116739:AA: 8/28206)	-	Oct 16, 2022 (156)
60	ALFA	NC_000011.10 - 101116740	Apr 26, 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)
rs147999965	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4241245990	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAA:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4241245989	NC_000011.10:101116739:AAAAA:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4241245988	NC_000011.10:101116739:AAA:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3792175095, ss5203571723	NC_000011.9:100987470:AA:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245987, ss5288653658, ss5483667551, ss5751928426	NC_000011.10:101116739:AA:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294719160	NC_000011.8:100492680:A:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3008665726, ss3832802918, ss5203571721, ss5651931093	NC_000011.9:100987470:A:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5288653656, ss5483667552, ss5751928424	NC_000011.10:101116739:A:	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5203571722	NC_000011.9:100987470::A	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245973, ss5288653657, ss5483667553, ss5751928425	NC_000011.10:101116739::A	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245974, ss5483667554	NC_000011.10:101116739::AA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4065158486	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245975	NC_000011.10:101116739::AAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245976	NC_000011.10:101116739::AAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245977	NC_000011.10:101116739::AAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245978	NC_000011.10:101116739::AAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245979	NC_000011.10:101116739::AAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245980	NC_000011.10:101116739::AAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245981	NC_000011.10:101116739::AAAAAAAAAA… NC_000011.10:101116739::AAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245982	NC_000011.10:101116739::AAAAAAAAAA… NC_000011.10:101116739::AAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245983	NC_000011.10:101116739::AAAAAAAAAA… NC_000011.10:101116739::AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245984	NC_000011.10:101116739::AAAAAAAAAA… NC_000011.10:101116739::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4241245985	NC_000011.10:101116739::AAAAAAAAAA… NC_000011.10:101116739::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:101116739:AAAAAAAAAAA… NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11300466

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

rs11300466