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dbSNP Short Genetic Variations

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.

rs57973366

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:181149522-181149549 (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(AT)7 / del(AT)6 / del(AT)5 / d…

del(AT)7 / del(AT)6 / del(AT)5 / del(AT)4 / del(AT)3 / delATAT / delAT / dupAT / dupATAT / dup(AT)3 / dup(AT)4 / dup(AT)5 / dup(AT)6 / dup(AT)7 / dup(AT)8 / dup(AT)9

Variation Type
Indel Insertion and Deletion
Frequency
del(AT)7=0.00000 (0/11536, ALFA)
del(AT)6=0.00000 (0/11536, ALFA)
del(AT)5=0.00000 (0/11536, ALFA) (+ 9 more)
del(AT)4=0.00000 (0/11536, ALFA)
del(AT)3=0.00000 (0/11536, ALFA)
delATAT=0.00000 (0/11536, ALFA)
delAT=0.00000 (0/11536, ALFA)
dupAT=0.00000 (0/11536, ALFA)
dupATAT=0.00000 (0/11536, ALFA)
dup(AT)3=0.00000 (0/11536, ALFA)
dup(AT)4=0.00000 (0/11536, ALFA)
dup(AT)7=0.00000 (0/11536, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LINC00290 : 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 11536 ATATATATATATATATATATATATATAT=1.00000 ATATATATATATAT=0.00000, ATATATATATATATAT=0.00000, ATATATATATATATATAT=0.00000, ATATATATATATATATATAT=0.00000, ATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATATATATATATATAT=0.00000, ATATATATATATATATATATATATATATATATATATATATAT=0.00000 1.0 0.0 0.0 N/A
European Sub 7506 ATATATATATATATATATATATATATAT=1.0000 ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATAT=0.0000 1.0 0.0 0.0 N/A
African Sub 2648 ATATATATATATATATATATATATATAT=1.0000 ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATAT=0.0000 1.0 0.0 0.0 N/A
African Others Sub 96 ATATATATATATATATATATATATATAT=1.00 ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00 1.0 0.0 0.0 N/A
African American Sub 2552 ATATATATATATATATATATATATATAT=1.0000 ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATAT=0.0000 1.0 0.0 0.0 N/A
Asian Sub 106 ATATATATATATATATATATATATATAT=1.000 ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000 1.0 0.0 0.0 N/A
East Asian Sub 84 ATATATATATATATATATATATATATAT=1.00 ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 22 ATATATATATATATATATATATATATAT=1.00 ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 142 ATATATATATATATATATATATATATAT=1.000 ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 584 ATATATATATATATATATATATATATAT=1.000 ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000 1.0 0.0 0.0 N/A
South Asian Sub 90 ATATATATATATATATATATATATATAT=1.00 ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00 1.0 0.0 0.0 N/A
Other Sub 460 ATATATATATATATATATATATATATAT=1.000 ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000 1.0 0.0 0.0 N/A


Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
Allele Frequency Aggregator Total Global 11536 (AT)14=1.00000 del(AT)7=0.00000, del(AT)6=0.00000, del(AT)5=0.00000, del(AT)4=0.00000, del(AT)3=0.00000, delATAT=0.00000, delAT=0.00000, dupAT=0.00000, dupATAT=0.00000, dup(AT)3=0.00000, dup(AT)4=0.00000, dup(AT)7=0.00000
Allele Frequency Aggregator European Sub 7506 (AT)14=1.0000 del(AT)7=0.0000, del(AT)6=0.0000, del(AT)5=0.0000, del(AT)4=0.0000, del(AT)3=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)3=0.0000, dup(AT)4=0.0000, dup(AT)7=0.0000
Allele Frequency Aggregator African Sub 2648 (AT)14=1.0000 del(AT)7=0.0000, del(AT)6=0.0000, del(AT)5=0.0000, del(AT)4=0.0000, del(AT)3=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)3=0.0000, dup(AT)4=0.0000, dup(AT)7=0.0000
Allele Frequency Aggregator Latin American 2 Sub 584 (AT)14=1.000 del(AT)7=0.000, del(AT)6=0.000, del(AT)5=0.000, del(AT)4=0.000, del(AT)3=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)3=0.000, dup(AT)4=0.000, dup(AT)7=0.000
Allele Frequency Aggregator Other Sub 460 (AT)14=1.000 del(AT)7=0.000, del(AT)6=0.000, del(AT)5=0.000, del(AT)4=0.000, del(AT)3=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)3=0.000, dup(AT)4=0.000, dup(AT)7=0.000
Allele Frequency Aggregator Latin American 1 Sub 142 (AT)14=1.000 del(AT)7=0.000, del(AT)6=0.000, del(AT)5=0.000, del(AT)4=0.000, del(AT)3=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)3=0.000, dup(AT)4=0.000, dup(AT)7=0.000
Allele Frequency Aggregator Asian Sub 106 (AT)14=1.000 del(AT)7=0.000, del(AT)6=0.000, del(AT)5=0.000, del(AT)4=0.000, del(AT)3=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)3=0.000, dup(AT)4=0.000, dup(AT)7=0.000
Allele Frequency Aggregator South Asian Sub 90 (AT)14=1.00 del(AT)7=0.00, del(AT)6=0.00, del(AT)5=0.00, del(AT)4=0.00, del(AT)3=0.00, delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00, dup(AT)3=0.00, dup(AT)4=0.00, dup(AT)7=0.00
Help

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 4 NC_000004.12:g.181149522AT[7]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[8]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[9]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[10]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[11]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[12]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[13]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[15]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[16]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[17]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[18]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[19]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[20]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[21]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[22]
GRCh38.p14 chr 4 NC_000004.12:g.181149522AT[23]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[7]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[8]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[9]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[10]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[11]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[12]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[13]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[15]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[16]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[17]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[18]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[19]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[20]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[21]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[22]
GRCh37.p13 chr 4 NC_000004.11:g.182070675AT[23]
Gene: LINC00290, long intergenic non-protein coding RNA 290 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LINC00290 transcript NR_033918.1:n. N/A Intron Variant
Help

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
Help

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 (AT)14= del(AT)7 del(AT)6 del(AT)5 del(AT)4 del(AT)3 delATAT delAT dupAT dupATAT dup(AT)3 dup(AT)4 dup(AT)5 dup(AT)6 dup(AT)7 dup(AT)8 dup(AT)9
GRCh38.p14 chr 4 NC_000004.12:g.181149522_181149549= NC_000004.12:g.181149522AT[7] NC_000004.12:g.181149522AT[8] NC_000004.12:g.181149522AT[9] NC_000004.12:g.181149522AT[10] NC_000004.12:g.181149522AT[11] NC_000004.12:g.181149522AT[12] NC_000004.12:g.181149522AT[13] NC_000004.12:g.181149522AT[15] NC_000004.12:g.181149522AT[16] NC_000004.12:g.181149522AT[17] NC_000004.12:g.181149522AT[18] NC_000004.12:g.181149522AT[19] NC_000004.12:g.181149522AT[20] NC_000004.12:g.181149522AT[21] NC_000004.12:g.181149522AT[22] NC_000004.12:g.181149522AT[23]
GRCh37.p13 chr 4 NC_000004.11:g.182070675_182070702= NC_000004.11:g.182070675AT[7] NC_000004.11:g.182070675AT[8] NC_000004.11:g.182070675AT[9] NC_000004.11:g.182070675AT[10] NC_000004.11:g.182070675AT[11] NC_000004.11:g.182070675AT[12] NC_000004.11:g.182070675AT[13] NC_000004.11:g.182070675AT[15] NC_000004.11:g.182070675AT[16] NC_000004.11:g.182070675AT[17] NC_000004.11:g.182070675AT[18] NC_000004.11:g.182070675AT[19] NC_000004.11:g.182070675AT[20] NC_000004.11:g.182070675AT[21] NC_000004.11:g.182070675AT[22] NC_000004.11:g.182070675AT[23]
Help

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#.

34 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 HGSV ss80891656 Dec 14, 2007 (129)
2 HGSV ss80902187 Dec 14, 2007 (129)
3 MCHAISSO ss3065007399 Nov 08, 2017 (151)
4 EVA_DECODE ss3713781073 Jul 13, 2019 (153)
5 EVA_DECODE ss3713781074 Jul 13, 2019 (153)
6 EVA_DECODE ss3713781075 Jul 13, 2019 (153)
7 EVA_DECODE ss3713781076 Jul 13, 2019 (153)
8 EVA_DECODE ss3713781077 Jul 13, 2019 (153)
9 EVA_DECODE ss3713781078 Jul 13, 2019 (153)
10 GNOMAD ss4096737455 Apr 26, 2021 (155)
11 GNOMAD ss4096737456 Apr 26, 2021 (155)
12 GNOMAD ss4096737457 Apr 26, 2021 (155)
13 GNOMAD ss4096737458 Apr 26, 2021 (155)
14 GNOMAD ss4096737459 Apr 26, 2021 (155)
15 GNOMAD ss4096737460 Apr 26, 2021 (155)
16 GNOMAD ss4096737461 Apr 26, 2021 (155)
17 GNOMAD ss4096737462 Apr 26, 2021 (155)
18 TOMMO_GENOMICS ss5169643154 Apr 26, 2021 (155)
19 TOMMO_GENOMICS ss5169643155 Apr 26, 2021 (155)
20 TOMMO_GENOMICS ss5169643156 Apr 26, 2021 (155)
21 TOMMO_GENOMICS ss5169643157 Apr 26, 2021 (155)
22 TOMMO_GENOMICS ss5169643158 Apr 26, 2021 (155)
23 TOMMO_GENOMICS ss5169643159 Apr 26, 2021 (155)
24 1000G_HIGH_COVERAGE ss5262304831 Oct 13, 2022 (156)
25 1000G_HIGH_COVERAGE ss5262304832 Oct 13, 2022 (156)
26 1000G_HIGH_COVERAGE ss5262304833 Oct 13, 2022 (156)
27 1000G_HIGH_COVERAGE ss5262304834 Oct 13, 2022 (156)
28 1000G_HIGH_COVERAGE ss5262304835 Oct 13, 2022 (156)
29 TOMMO_GENOMICS ss5705084329 Oct 13, 2022 (156)
30 TOMMO_GENOMICS ss5705084330 Oct 13, 2022 (156)
31 TOMMO_GENOMICS ss5705084331 Oct 13, 2022 (156)
32 TOMMO_GENOMICS ss5705084332 Oct 13, 2022 (156)
33 TOMMO_GENOMICS ss5705084333 Oct 13, 2022 (156)
34 TOMMO_GENOMICS ss5705084334 Oct 13, 2022 (156)
35 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
36 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
37 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
38 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
39 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
40 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
41 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
42 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 175559035 (NC_000004.12:181149521::AT 14/25094)
Row 175559036 (NC_000004.12:181149521::ATAT 10/25096)
Row 175559037 (NC_000004.12:181149521::ATATAT 15/25088)...

- Apr 26, 2021 (155)
43 8.3KJPN

Submission ignored due to conflicting rows:
Row 27612461 (NC_000004.11:182070674:ATAT: 983/15922)
Row 27612462 (NC_000004.11:182070674::ATATATATATAT 882/15922)
Row 27612463 (NC_000004.11:182070674::ATATATATATATAT 569/15922)...

- Apr 26, 2021 (155)
44 8.3KJPN

Submission ignored due to conflicting rows:
Row 27612461 (NC_000004.11:182070674:ATAT: 983/15922)
Row 27612462 (NC_000004.11:182070674::ATATATATATAT 882/15922)
Row 27612463 (NC_000004.11:182070674::ATATATATATATAT 569/15922)...

- Apr 26, 2021 (155)
45 8.3KJPN

Submission ignored due to conflicting rows:
Row 27612461 (NC_000004.11:182070674:ATAT: 983/15922)
Row 27612462 (NC_000004.11:182070674::ATATATATATAT 882/15922)
Row 27612463 (NC_000004.11:182070674::ATATATATATATAT 569/15922)...

- Apr 26, 2021 (155)
46 8.3KJPN

Submission ignored due to conflicting rows:
Row 27612461 (NC_000004.11:182070674:ATAT: 983/15922)
Row 27612462 (NC_000004.11:182070674::ATATATATATAT 882/15922)
Row 27612463 (NC_000004.11:182070674::ATATATATATATAT 569/15922)...

- Apr 26, 2021 (155)
47 8.3KJPN

Submission ignored due to conflicting rows:
Row 27612461 (NC_000004.11:182070674:ATAT: 983/15922)
Row 27612462 (NC_000004.11:182070674::ATATATATATAT 882/15922)
Row 27612463 (NC_000004.11:182070674::ATATATATATATAT 569/15922)...

- Apr 26, 2021 (155)
48 8.3KJPN

Submission ignored due to conflicting rows:
Row 27612461 (NC_000004.11:182070674:ATAT: 983/15922)
Row 27612462 (NC_000004.11:182070674::ATATATATATAT 882/15922)
Row 27612463 (NC_000004.11:182070674::ATATATATATATAT 569/15922)...

- Apr 26, 2021 (155)
49 14KJPN

Submission ignored due to conflicting rows:
Row 38921433 (NC_000004.12:181149521:ATAT: 1167/25996)
Row 38921434 (NC_000004.12:181149521::ATATATATATATAT 644/25996)
Row 38921435 (NC_000004.12:181149521::ATATATATATATATAT 726/25996)...

- Oct 13, 2022 (156)
50 14KJPN

Submission ignored due to conflicting rows:
Row 38921433 (NC_000004.12:181149521:ATAT: 1167/25996)
Row 38921434 (NC_000004.12:181149521::ATATATATATATAT 644/25996)
Row 38921435 (NC_000004.12:181149521::ATATATATATATATAT 726/25996)...

- Oct 13, 2022 (156)
51 14KJPN

Submission ignored due to conflicting rows:
Row 38921433 (NC_000004.12:181149521:ATAT: 1167/25996)
Row 38921434 (NC_000004.12:181149521::ATATATATATATAT 644/25996)
Row 38921435 (NC_000004.12:181149521::ATATATATATATATAT 726/25996)...

- Oct 13, 2022 (156)
52 14KJPN

Submission ignored due to conflicting rows:
Row 38921433 (NC_000004.12:181149521:ATAT: 1167/25996)
Row 38921434 (NC_000004.12:181149521::ATATATATATATAT 644/25996)
Row 38921435 (NC_000004.12:181149521::ATATATATATATATAT 726/25996)...

- Oct 13, 2022 (156)
53 14KJPN

Submission ignored due to conflicting rows:
Row 38921433 (NC_000004.12:181149521:ATAT: 1167/25996)
Row 38921434 (NC_000004.12:181149521::ATATATATATATAT 644/25996)
Row 38921435 (NC_000004.12:181149521::ATATATATATATATAT 726/25996)...

- Oct 13, 2022 (156)
54 14KJPN

Submission ignored due to conflicting rows:
Row 38921433 (NC_000004.12:181149521:ATAT: 1167/25996)
Row 38921434 (NC_000004.12:181149521::ATATATATATATAT 644/25996)
Row 38921435 (NC_000004.12:181149521::ATATATATATATATAT 726/25996)...

- Oct 13, 2022 (156)
55 ALFA NC_000004.12 - 181149522 Apr 26, 2021 (155)
Help

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)
rs72154985 May 11, 2012 (137)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATAT

(self)
ss4096737462 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATAT:

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATAT

(self)
ss4096737461 NC_000004.12:181149521:ATATATATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATAT

(self)
ss5169643158 NC_000004.11:182070674:ATATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATAT

(self)
ss3713781078, ss4096737460, ss5262304832, ss5705084334 NC_000004.12:181149521:ATATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATAT

(self)
ss5169643154 NC_000004.11:182070674:ATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT

(self)
ss3065007399, ss4096737459, ss5705084329 NC_000004.12:181149521:ATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT

(self)
ss3713781077 NC_000004.12:181149523:ATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT

(self)
ss80891656, ss80902187 NC_000004.9:182445849:AT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT

(self)
ss4096737458 NC_000004.12:181149521:AT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT

(self)
ss3713781076 NC_000004.12:181149525:AT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT

(self)
ss4096737455 NC_000004.12:181149521::AT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT

(self)
ss4096737456 NC_000004.12:181149521::ATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT

(self)
ss4096737457 NC_000004.12:181149521::ATATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT

(self)
ss3713781075 NC_000004.12:181149527::ATATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT

(self)
10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT

(self)
ss3713781074 NC_000004.12:181149527::ATATATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT

(self)
ss5262304831 NC_000004.12:181149521::ATATATATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT

ss3713781073 NC_000004.12:181149527::ATATATATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT

(self)
ss5169643155 NC_000004.11:182070674::ATATATATAT…

NC_000004.11:182070674::ATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT

(self)
ss5262304835, ss5705084332 NC_000004.12:181149521::ATATATATAT…

NC_000004.12:181149521::ATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT

ss5169643156 NC_000004.11:182070674::ATATATATAT…

NC_000004.11:182070674::ATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT

(self)
ss5262304833, ss5705084330 NC_000004.12:181149521::ATATATATAT…

NC_000004.12:181149521::ATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT

10778324379 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT

(self)
ss5169643157 NC_000004.11:182070674::ATATATATAT…

NC_000004.11:182070674::ATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT

(self)
ss5262304834, ss5705084331 NC_000004.12:181149521::ATATATATAT…

NC_000004.12:181149521::ATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT

ss5169643159 NC_000004.11:182070674::ATATATATAT…

NC_000004.11:182070674::ATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT

(self)
ss5705084333 NC_000004.12:181149521::ATATATATAT…

NC_000004.12:181149521::ATATATATATATATATAT

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT

Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3452273102 NC_000004.12:181149521::ATATATAT NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT

ss3452273107 NC_000004.12:181149521:ATATATAT: NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATAT

ss3452273109 NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATAT:

NC_000004.12:181149521:ATATATATATA…

NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATAT

Help

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

No publications for rs57973366

Help

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.

Software version is: 2.0.1.post820+afb47a3d