Name: rs57385993
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.

rs57385993

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:2419449-2419467 (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)₁₀ / del(A)₉ / del(A)₈ / del…
del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₉=0.4161 (2084/5008, 1000G)
del(A)₁₀=0.0000 (0/1120, ALFA)
del(A)₉=0.0000 (0/1120, ALFA) (+ 9 more)
del(A)₈=0.0000 (0/1120, ALFA)
del(A)₇=0.0000 (0/1120, ALFA)
del(A)₆=0.0000 (0/1120, ALFA)
del(A)₅=0.0000 (0/1120, ALFA)
del(A)₄=0.0000 (0/1120, ALFA)
delAAA=0.0000 (0/1120, ALFA)
delAA=0.0000 (0/1120, ALFA)
delA=0.0000 (0/1120, ALFA)
dupA=0.0000 (0/1120, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRPM5 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	1120	AAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	942	AAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	112	AAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	110	AAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	6	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	20	AAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	34	AAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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
1000Genomes	Global	Study-wide	5008	(A)₁₉=0.4161	del(A)₅=0.5839
1000Genomes	African	Sub	1322	(A)₁₉=0.2935	del(A)₅=0.7065
1000Genomes	East Asian	Sub	1008	(A)₁₉=0.2946	del(A)₅=0.7054
1000Genomes	Europe	Sub	1006	(A)₁₉=0.6203	del(A)₅=0.3797
1000Genomes	South Asian	Sub	978	(A)₁₉=0.490	del(A)₅=0.510
1000Genomes	American	Sub	694	(A)₁₉=0.427	del(A)₅=0.573
Allele Frequency Aggregator	Total	Global	1120	(A)₁₉=1.0000	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)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	European	Sub	942	(A)₁₉=1.000	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)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	African	Sub	112	(A)₁₉=1.000	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)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	34	(A)₁₉=1.00	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)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	20	(A)₁₉=1.00	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)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	6	(A)₁₉=1.0	del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	South Asian	Sub	6	(A)₁₉=1.0	del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₉=0	del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0

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.2419458_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419459_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419460_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419461_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419462_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419463_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419464_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419465_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419466_2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419467del
GRCh38.p14 chr 11	NC_000011.10:g.2419467dup
GRCh38.p14 chr 11	NC_000011.10:g.2419466_2419467dup
GRCh37.p13 chr 11	NC_000011.9:g.2440688_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440689_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440690_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440691_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440692_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440693_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440694_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440695_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440696_2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440697del
GRCh37.p13 chr 11	NC_000011.9:g.2440697dup
GRCh37.p13 chr 11	NC_000011.9:g.2440696_2440697dup

Gene: TRPM5, transient receptor potential cation channel subfamily M member 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TRPM5 transcript	NM_014555.4:c.649+764_649… NM_014555.4:c.649+764_649+773del	N/A	Intron Variant
TRPM5 transcript variant X2	XM_017017628.2:c.703+764_… XM_017017628.2:c.703+764_703+773del	N/A	Intron Variant
TRPM5 transcript variant X3	XM_047426858.1:c.703+764_… XM_047426858.1:c.703+764_703+773del	N/A	Intron Variant
TRPM5 transcript variant X1	XM_047426859.1:c.	N/A	Genic Upstream Transcript 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)₁₉=	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 11	NC_000011.10:g.2419449_2419467=	NC_000011.10:g.2419458_2419467del	NC_000011.10:g.2419459_2419467del	NC_000011.10:g.2419460_2419467del	NC_000011.10:g.2419461_2419467del	NC_000011.10:g.2419462_2419467del	NC_000011.10:g.2419463_2419467del	NC_000011.10:g.2419464_2419467del	NC_000011.10:g.2419465_2419467del	NC_000011.10:g.2419466_2419467del	NC_000011.10:g.2419467del	NC_000011.10:g.2419467dup	NC_000011.10:g.2419466_2419467dup
GRCh37.p13 chr 11	NC_000011.9:g.2440679_2440697=	NC_000011.9:g.2440688_2440697del	NC_000011.9:g.2440689_2440697del	NC_000011.9:g.2440690_2440697del	NC_000011.9:g.2440691_2440697del	NC_000011.9:g.2440692_2440697del	NC_000011.9:g.2440693_2440697del	NC_000011.9:g.2440694_2440697del	NC_000011.9:g.2440695_2440697del	NC_000011.9:g.2440696_2440697del	NC_000011.9:g.2440697del	NC_000011.9:g.2440697dup	NC_000011.9:g.2440696_2440697dup
TRPM5 transcript	NM_014555.3:c.649+773=	NM_014555.3:c.649+764_649+773del	NM_014555.3:c.649+765_649+773del	NM_014555.3:c.649+766_649+773del	NM_014555.3:c.649+767_649+773del	NM_014555.3:c.649+768_649+773del	NM_014555.3:c.649+769_649+773del	NM_014555.3:c.649+770_649+773del	NM_014555.3:c.649+771_649+773del	NM_014555.3:c.649+772_649+773del	NM_014555.3:c.649+773del	NM_014555.3:c.649+773dup	NM_014555.3:c.649+772_649+773dup
TRPM5 transcript	NM_014555.4:c.649+773=	NM_014555.4:c.649+764_649+773del	NM_014555.4:c.649+765_649+773del	NM_014555.4:c.649+766_649+773del	NM_014555.4:c.649+767_649+773del	NM_014555.4:c.649+768_649+773del	NM_014555.4:c.649+769_649+773del	NM_014555.4:c.649+770_649+773del	NM_014555.4:c.649+771_649+773del	NM_014555.4:c.649+772_649+773del	NM_014555.4:c.649+773del	NM_014555.4:c.649+773dup	NM_014555.4:c.649+772_649+773dup
TRPM5 transcript variant X1	XM_005252881.1:c.649+773=	XM_005252881.1:c.649+764_649+773del	XM_005252881.1:c.649+765_649+773del	XM_005252881.1:c.649+766_649+773del	XM_005252881.1:c.649+767_649+773del	XM_005252881.1:c.649+768_649+773del	XM_005252881.1:c.649+769_649+773del	XM_005252881.1:c.649+770_649+773del	XM_005252881.1:c.649+771_649+773del	XM_005252881.1:c.649+772_649+773del	XM_005252881.1:c.649+773del	XM_005252881.1:c.649+773dup	XM_005252881.1:c.649+772_649+773dup
TRPM5 transcript variant X2	XM_005252882.1:c.649+773=	XM_005252882.1:c.649+764_649+773del	XM_005252882.1:c.649+765_649+773del	XM_005252882.1:c.649+766_649+773del	XM_005252882.1:c.649+767_649+773del	XM_005252882.1:c.649+768_649+773del	XM_005252882.1:c.649+769_649+773del	XM_005252882.1:c.649+770_649+773del	XM_005252882.1:c.649+771_649+773del	XM_005252882.1:c.649+772_649+773del	XM_005252882.1:c.649+773del	XM_005252882.1:c.649+773dup	XM_005252882.1:c.649+772_649+773dup
TRPM5 transcript variant X2	XM_017017628.2:c.703+773=	XM_017017628.2:c.703+764_703+773del	XM_017017628.2:c.703+765_703+773del	XM_017017628.2:c.703+766_703+773del	XM_017017628.2:c.703+767_703+773del	XM_017017628.2:c.703+768_703+773del	XM_017017628.2:c.703+769_703+773del	XM_017017628.2:c.703+770_703+773del	XM_017017628.2:c.703+771_703+773del	XM_017017628.2:c.703+772_703+773del	XM_017017628.2:c.703+773del	XM_017017628.2:c.703+773dup	XM_017017628.2:c.703+772_703+773dup
TRPM5 transcript variant X3	XM_047426858.1:c.703+773=	XM_047426858.1:c.703+764_703+773del	XM_047426858.1:c.703+765_703+773del	XM_047426858.1:c.703+766_703+773del	XM_047426858.1:c.703+767_703+773del	XM_047426858.1:c.703+768_703+773del	XM_047426858.1:c.703+769_703+773del	XM_047426858.1:c.703+770_703+773del	XM_047426858.1:c.703+771_703+773del	XM_047426858.1:c.703+772_703+773del	XM_047426858.1:c.703+773del	XM_047426858.1:c.703+773dup	XM_047426858.1:c.703+772_703+773dup

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#.

67 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79957547	Dec 14, 2007 (129)
2	HUMANGENOME_JCVI	ss95558502	Mar 15, 2016 (147)
3	BCMHGSC_JDW	ss103519062	Dec 01, 2009 (131)
4	BUSHMAN	ss193214598	Apr 25, 2013 (138)
5	PJP	ss294685595	May 31, 2013 (142)
6	PJP	ss294685596	May 09, 2011 (134)
7	SSMP	ss664041974	Apr 01, 2015 (144)
8	BILGI_BIOE	ss666522166	Apr 25, 2013 (138)
9	1000GENOMES	ss1370417526	Aug 21, 2014 (142)
10	EVA_UK10K_ALSPAC	ss1706971743	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1706971753	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710497256	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710497258	Apr 01, 2015 (144)
14	SWEGEN	ss3007478879	Nov 08, 2017 (151)
15	MCHAISSO	ss3063677484	Jan 10, 2018 (151)
16	URBANLAB	ss3649514272	Oct 12, 2018 (152)
17	EVA_DECODE	ss3691081032	Jul 13, 2019 (153)
18	EVA_DECODE	ss3691081033	Jul 13, 2019 (153)
19	EVA_DECODE	ss3691081034	Jul 13, 2019 (153)
20	EVA_DECODE	ss3691081035	Jul 13, 2019 (153)
21	EVA_DECODE	ss3691081036	Jul 13, 2019 (153)
22	ACPOP	ss3737856704	Jul 13, 2019 (153)
23	ACPOP	ss3737856705	Jul 13, 2019 (153)
24	PACBIO	ss3786843885	Jul 13, 2019 (153)
25	PACBIO	ss3792000247	Jul 13, 2019 (153)
26	PACBIO	ss3796882424	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3814205145	Jul 13, 2019 (153)
28	EVA	ss3832438599	Apr 26, 2020 (154)
29	KOGIC	ss3969071551	Apr 26, 2020 (154)
30	KOGIC	ss3969071552	Apr 26, 2020 (154)
31	KOGIC	ss3969071553	Apr 26, 2020 (154)
32	KOGIC	ss3969071554	Apr 26, 2020 (154)
33	KOGIC	ss3969071555	Apr 26, 2020 (154)
34	KOGIC	ss3969071556	Apr 26, 2020 (154)
35	GNOMAD	ss4228931604	Apr 26, 2021 (155)
36	GNOMAD	ss4228931605	Apr 26, 2021 (155)
37	GNOMAD	ss4228931606	Apr 26, 2021 (155)
38	GNOMAD	ss4228931607	Apr 26, 2021 (155)
39	GNOMAD	ss4228931608	Apr 26, 2021 (155)
40	GNOMAD	ss4228931609	Apr 26, 2021 (155)
41	GNOMAD	ss4228931610	Apr 26, 2021 (155)
42	GNOMAD	ss4228931611	Apr 26, 2021 (155)
43	GNOMAD	ss4228931612	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5200377370	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5200377371	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5200377372	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5200377373	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5200377374	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5286160601	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5286160602	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5286160603	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5286160604	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5286160605	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5286160606	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5481501354	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5481501355	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5481501356	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5481501357	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5747045831	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5747045832	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5747045833	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5747045834	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5747045835	Oct 16, 2022 (156)
64	EVA	ss5836164697	Oct 16, 2022 (156)
65	EVA	ss5836164698	Oct 16, 2022 (156)
66	EVA	ss5849828522	Oct 16, 2022 (156)
67	EVA	ss5918564061	Oct 16, 2022 (156)
68	1000Genomes	NC_000011.9 - 2440679	Oct 12, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29065018 (NC_000011.9:2440679:AAAA: 3123/3854) Row 29065019 (NC_000011.9:2440678:AAAAAA: 213/3854)	-	Oct 12, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29065018 (NC_000011.9:2440679:AAAA: 3123/3854) Row 29065019 (NC_000011.9:2440678:AAAAAA: 213/3854)	-	Oct 12, 2018 (152)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369458904 (NC_000011.10:2419448::A 67/126384) Row 369458905 (NC_000011.10:2419448::AA 1/126382) Row 369458906 (NC_000011.10:2419448:A: 30091/125662)...	-	Apr 26, 2021 (155)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 25449552 (NC_000011.10:2419449:AAAAA: 1159/1826) Row 25449553 (NC_000011.10:2419448:AAAAAA: 56/1826) Row 25449554 (NC_000011.10:2419450:AAAA: 35/1826)...	-	Apr 26, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 25449552 (NC_000011.10:2419449:AAAAA: 1159/1826) Row 25449553 (NC_000011.10:2419448:AAAAAA: 56/1826) Row 25449554 (NC_000011.10:2419450:AAAA: 35/1826)...	-	Apr 26, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 25449552 (NC_000011.10:2419449:AAAAA: 1159/1826) Row 25449553 (NC_000011.10:2419448:AAAAAA: 56/1826) Row 25449554 (NC_000011.10:2419450:AAAA: 35/1826)...	-	Apr 26, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 25449552 (NC_000011.10:2419449:AAAAA: 1159/1826) Row 25449553 (NC_000011.10:2419448:AAAAAA: 56/1826) Row 25449554 (NC_000011.10:2419450:AAAA: 35/1826)...	-	Apr 26, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 25449552 (NC_000011.10:2419449:AAAAA: 1159/1826) Row 25449553 (NC_000011.10:2419448:AAAAAA: 56/1826) Row 25449554 (NC_000011.10:2419450:AAAA: 35/1826)...	-	Apr 26, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 25449552 (NC_000011.10:2419449:AAAAA: 1159/1826) Row 25449553 (NC_000011.10:2419448:AAAAAA: 56/1826) Row 25449554 (NC_000011.10:2419450:AAAA: 35/1826)...	-	Apr 26, 2020 (154)
86	Northern Sweden Submission ignored due to conflicting rows: Row 11141569 (NC_000011.9:2440678:AAAAA: 233/562) Row 11141570 (NC_000011.9:2440678:A: 72/562)	-	Jul 13, 2019 (153)
87	Northern Sweden Submission ignored due to conflicting rows: Row 11141569 (NC_000011.9:2440678:AAAAA: 233/562) Row 11141570 (NC_000011.9:2440678:A: 72/562)	-	Jul 13, 2019 (153)
88	8.3KJPN Submission ignored due to conflicting rows: Row 58346677 (NC_000011.9:2440678:AAAAA: 12267/16660) Row 58346678 (NC_000011.9:2440678:A: 2249/16660) Row 58346679 (NC_000011.9:2440678:AAAAAA: 53/16660)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 58346677 (NC_000011.9:2440678:AAAAA: 12267/16660) Row 58346678 (NC_000011.9:2440678:A: 2249/16660) Row 58346679 (NC_000011.9:2440678:AAAAAA: 53/16660)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 58346677 (NC_000011.9:2440678:AAAAA: 12267/16660) Row 58346678 (NC_000011.9:2440678:A: 2249/16660) Row 58346679 (NC_000011.9:2440678:AAAAAA: 53/16660)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 58346677 (NC_000011.9:2440678:AAAAA: 12267/16660) Row 58346678 (NC_000011.9:2440678:A: 2249/16660) Row 58346679 (NC_000011.9:2440678:AAAAAA: 53/16660)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 58346677 (NC_000011.9:2440678:AAAAA: 12267/16660) Row 58346678 (NC_000011.9:2440678:A: 2249/16660) Row 58346679 (NC_000011.9:2440678:AAAAAA: 53/16660)...	-	Apr 26, 2021 (155)
93	14KJPN Submission ignored due to conflicting rows: Row 80882935 (NC_000011.10:2419448:AAAAA: 21188/28180) Row 80882936 (NC_000011.10:2419448:A: 3571/28180) Row 80882937 (NC_000011.10:2419448:AAAAAA: 91/28180)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 80882935 (NC_000011.10:2419448:AAAAA: 21188/28180) Row 80882936 (NC_000011.10:2419448:A: 3571/28180) Row 80882937 (NC_000011.10:2419448:AAAAAA: 91/28180)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 80882935 (NC_000011.10:2419448:AAAAA: 21188/28180) Row 80882936 (NC_000011.10:2419448:A: 3571/28180) Row 80882937 (NC_000011.10:2419448:AAAAAA: 91/28180)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 80882935 (NC_000011.10:2419448:AAAAA: 21188/28180) Row 80882936 (NC_000011.10:2419448:A: 3571/28180) Row 80882937 (NC_000011.10:2419448:AAAAAA: 91/28180)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 80882935 (NC_000011.10:2419448:AAAAA: 21188/28180) Row 80882936 (NC_000011.10:2419448:A: 3571/28180) Row 80882937 (NC_000011.10:2419448:AAAAAA: 91/28180)...	-	Oct 16, 2022 (156)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29065018 (NC_000011.9:2440679:AAAA: 3001/3708) Row 29065019 (NC_000011.9:2440678:AAAAAA: 143/3708)	-	Oct 12, 2018 (152)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29065018 (NC_000011.9:2440679:AAAA: 3001/3708) Row 29065019 (NC_000011.9:2440678:AAAAAA: 143/3708)	-	Oct 12, 2018 (152)
100	ALFA	NC_000011.10 - 2419449	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)
rs386372928	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4228931612	NC_000011.10:2419448:AAAAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss1706971743, ss1706971753, ss3786843885, ss5200377372, ss5836164698	NC_000011.9:2440678:AAAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3691081036, ss3969071552, ss4228931611, ss5286160604, ss5481501356, ss5747045833	NC_000011.10:2419448:AAAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss103519062	NT_009237.18:2380691:AAAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss294685595	NC_000011.8:2397254:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss294685596	NC_000011.8:2397268:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
52317300, ss664041974, ss666522166, ss1370417526, ss3007478879, ss3737856704, ss3792000247, ss3796882424, ss3832438599, ss5200377370, ss5836164697	NC_000011.9:2440678:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710497256, ss1710497258	NC_000011.9:2440679:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3649514272, ss3814205145, ss4228931610, ss5286160601, ss5481501354, ss5747045831, ss5849828522, ss5918564061	NC_000011.10:2419448:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3691081035, ss3969071551	NC_000011.10:2419449:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95558502	NT_009237.18:2380692:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss193214598	NT_009237.19:2359448:AAAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
	NC_000011.9:2440679:AAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4228931609, ss5286160605	NC_000011.10:2419448:AAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3691081034, ss3969071553	NC_000011.10:2419450:AAAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4228931608	NC_000011.10:2419448:AAA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5200377373	NC_000011.9:2440678:AA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3063677484, ss4228931607, ss5286160603, ss5481501357, ss5747045834	NC_000011.10:2419448:AA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3691081033, ss3969071554	NC_000011.10:2419452:AA:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss79957547	NC_000011.8:2397272:A:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3737856705, ss5200377371	NC_000011.9:2440678:A:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4228931606, ss5286160602, ss5481501355, ss5747045832	NC_000011.10:2419448:A:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3691081032, ss3969071555	NC_000011.10:2419453:A:	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5200377374	NC_000011.9:2440678::A	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4228931604, ss5286160606, ss5747045835	NC_000011.10:2419448::A	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10126960538	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3969071556	NC_000011.10:2419454::A	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4228931605	NC_000011.10:2419448::AA	NC_000011.10:2419448:AAAAAAAAAAAAA… NC_000011.10:2419448:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(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 rs57385993

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

rs57385993