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dbSNP Short Genetic Variations

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.

rs2857449

Current Build 152

Released October 2, 2018

Organism
Homo sapiens
Position
chr6:30164848 (GRCh38.p12) 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
G>A / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.02120 (2662/125568, TOPMED)
A=0.0220 (682/30936, GnomAD)
A=0.026 (132/5008, 1000G) (+ 3 more)
A=0.015 (65/4480, Estonian)
A=0.007 (26/3854, ALSPAC)
A=0.009 (33/3708, TWINSUK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRIM15 : Intron Variant
TRIM10 : 2KB Upstream Variant
Publications
0 citations
Genomic View
See rs on genome
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.p12 chr 6 NC_000006.12:g.30164848G>A
GRCh38.p12 chr 6 NC_000006.12:g.30164848G>C
GRCh38.p12 chr 6 NC_000006.12:g.30164848G>T
GRCh37.p13 chr 6 NC_000006.11:g.30132625G>A
GRCh37.p13 chr 6 NC_000006.11:g.30132625G>C
GRCh37.p13 chr 6 NC_000006.11:g.30132625G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1644646G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1644646G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1644646G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1644752G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1644752G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1644752G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1419976G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1419976G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1419976G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1425572G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1425572G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1425572G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1420749G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1420749G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1420749G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1426334G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1426334G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1426334G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1463779G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1463779G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1463779G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1463077G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1463077G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1463077G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1475550G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1475550G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1475550G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1481170G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1481170G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1481170G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1508921G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1508921G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1508921G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1514506G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1514506G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1514506G>T
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1422928G>A
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1422928G>C
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1422928G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1372844G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1372844G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1372844G>T
Gene: TRIM15, tripartite motif containing 15 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM15 transcript NM_033229.2:c. N/A Intron Variant
TRIM15 transcript variant X1 XM_011514987.1:c. N/A Intron Variant
TRIM15 transcript variant X2 XM_011514988.2:c. N/A Intron Variant
Gene: TRIM10, tripartite motif containing 10 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
TRIM10 transcript variant 1 NM_006778.3:c. N/A N/A
TRIM10 transcript variant 2 NM_052828.2:c. N/A N/A
TRIM10 transcript variant X1 XM_011514221.1:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X2 XM_011514222.2:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X3 XM_011514223.2:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X4 XM_011514225.1:c. N/A Upstream Transcript 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

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
TopMed Global Study-wide 125568 G=0.97880 A=0.02120
gnomAD - Genomes Global Study-wide 30936 G=0.9780 A=0.0220
gnomAD - Genomes European Sub 18478 G=0.9866 A=0.0134
gnomAD - Genomes African Sub 8718 G=0.957 A=0.043
gnomAD - Genomes East Asian Sub 1622 G=0.998 A=0.002
gnomAD - Genomes Other Sub 978 G=0.97 A=0.03
gnomAD - Genomes American Sub 838 G=0.98 A=0.02
gnomAD - Genomes Ashkenazi Jewish Sub 302 G=0.97 A=0.03
1000Genomes Global Study-wide 5008 G=0.974 A=0.026
1000Genomes African Sub 1322 G=0.953 A=0.047
1000Genomes East Asian Sub 1008 G=0.997 A=0.003
1000Genomes Europe Sub 1006 G=0.983 A=0.017
1000Genomes South Asian Sub 978 G=0.97 A=0.03
1000Genomes American Sub 694 G=0.97 A=0.03
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.985 A=0.015
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.993 A=0.007
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.991 A=0.009
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 G= A C T Note
GRCh38.p12 chr 6 NC_000006.12:...

NC_000006.12:g.30164848G=

NC_000006.12:...

NC_000006.12:g.30164848G>A

NC_000006.12:...

NC_000006.12:g.30164848G>C

NC_000006.12:...

NC_000006.12:g.30164848G>T

GRCh37.p13 chr 6 NC_000006.11:...

NC_000006.11:g.30132625G=

NC_000006.11:...

NC_000006.11:g.30132625G>A

NC_000006.11:...

NC_000006.11:g.30132625G>C

NC_000006.11:...

NC_000006.11:g.30132625G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g...

NT_113891.3:g.1644646G=

NT_113891.3:g...

NT_113891.3:g.1644646G>A

NT_113891.3:g...

NT_113891.3:g.1644646G>C

NT_113891.3:g...

NT_113891.3:g.1644646G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g...

NT_113891.2:g.1644752G=

NT_113891.2:g...

NT_113891.2:g.1644752G>A

NT_113891.2:g...

NT_113891.2:g.1644752G>C

NT_113891.2:g...

NT_113891.2:g.1644752G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g...

NT_167248.2:g.1419976G=

NT_167248.2:g...

NT_167248.2:g.1419976G>A

NT_167248.2:g...

NT_167248.2:g.1419976G>C

NT_167248.2:g...

NT_167248.2:g.1419976G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g...

NT_167248.1:g.1425572G=

NT_167248.1:g...

NT_167248.1:g.1425572G>A

NT_167248.1:g...

NT_167248.1:g.1425572G>C

NT_167248.1:g...

NT_167248.1:g.1425572G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g...

NT_167245.2:g.1420749G=

NT_167245.2:g...

NT_167245.2:g.1420749G>A

NT_167245.2:g...

NT_167245.2:g.1420749G>C

NT_167245.2:g...

NT_167245.2:g.1420749G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g...

NT_167245.1:g.1426334G=

NT_167245.1:g...

NT_167245.1:g.1426334G>A

NT_167245.1:g...

NT_167245.1:g.1426334G>C

NT_167245.1:g...

NT_167245.1:g.1426334G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g...

NT_167249.2:g.1463779G=

NT_167249.2:g...

NT_167249.2:g.1463779G>A

NT_167249.2:g...

NT_167249.2:g.1463779G>C

NT_167249.2:g...

NT_167249.2:g.1463779G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g...

NT_167249.1:g.1463077G=

NT_167249.1:g...

NT_167249.1:g.1463077G>A

NT_167249.1:g...

NT_167249.1:g.1463077G>C

NT_167249.1:g...

NT_167249.1:g.1463077G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g...

NT_167246.2:g.1475550G=

NT_167246.2:g...

NT_167246.2:g.1475550G>A

NT_167246.2:g...

NT_167246.2:g.1475550G>C

NT_167246.2:g...

NT_167246.2:g.1475550G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g...

NT_167246.1:g.1481170G=

NT_167246.1:g...

NT_167246.1:g.1481170G>A

NT_167246.1:g...

NT_167246.1:g.1481170G>C

NT_167246.1:g...

NT_167246.1:g.1481170G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g...

NT_167247.2:g.1508921G=

NT_167247.2:g...

NT_167247.2:g.1508921G>A

NT_167247.2:g...

NT_167247.2:g.1508921G>C

NT_167247.2:g...

NT_167247.2:g.1508921G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g...

NT_167247.1:g.1514506G=

NT_167247.1:g...

NT_167247.1:g.1514506G>A

NT_167247.1:g...

NT_167247.1:g.1514506G>C

NT_167247.1:g...

NT_167247.1:g.1514506G>T

GRCh38.p12 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g...

NT_167244.2:g.1422928G=

NT_167244.2:g...

NT_167244.2:g.1422928G>A

NT_167244.2:g...

NT_167244.2:g.1422928G>C

NT_167244.2:g...

NT_167244.2:g.1422928G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g...

NT_167244.1:g.1372844G=

NT_167244.1:g...

NT_167244.1:g.1372844G>A

NT_167244.1:g...

NT_167244.1:g.1372844G>C

NT_167244.1:g...

NT_167244.1:g.1372844G>T

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#.

55 SubSNP, 6 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss4045325 Sep 28, 2001 (100)
2 ILLUMINA ss67681233 Dec 02, 2006 (127)
3 ILLUMINA ss71331297 May 18, 2007 (127)
4 ILLUMINA ss75399948 Dec 07, 2007 (129)
5 KRIBB_YJKIM ss119448400 Dec 01, 2009 (131)
6 ILLUMINA ss160590835 Dec 01, 2009 (131)
7 ILLUMINA ss173506305 Jul 04, 2010 (132)
8 1000GENOMES ss222292064 Jul 14, 2010 (137)
9 1000GENOMES ss240458912 Jul 15, 2010 (137)
10 ILLUMINA ss480696398 May 04, 2012 (137)
11 ILLUMINA ss480711969 May 04, 2012 (137)
12 ILLUMINA ss481577808 Sep 08, 2015 (146)
13 ILLUMINA ss485143022 May 04, 2012 (137)
14 ILLUMINA ss535445556 Sep 08, 2015 (146)
15 SSMP ss653019000 Apr 25, 2013 (138)
16 ILLUMINA ss778509864 Aug 21, 2014 (142)
17 ILLUMINA ss783017802 Aug 21, 2014 (142)
18 ILLUMINA ss783977849 Aug 21, 2014 (142)
19 ILLUMINA ss832275270 Apr 01, 2015 (144)
20 ILLUMINA ss833966096 Aug 21, 2014 (142)
21 EVA-GONL ss982744503 Aug 21, 2014 (142)
22 1000GENOMES ss1319512492 Aug 21, 2014 (142)
23 EVA_GENOME_DK ss1581596323 Apr 01, 2015 (144)
24 EVA_DECODE ss1592291876 Apr 01, 2015 (144)
25 EVA_UK10K_ALSPAC ss1615251155 Apr 01, 2015 (144)
26 EVA_UK10K_TWINSUK ss1658245188 Apr 01, 2015 (144)
27 EVA_SVP ss1712848627 Apr 01, 2015 (144)
28 ILLUMINA ss1752625371 Sep 08, 2015 (146)
29 WEILL_CORNELL_DGM ss1925996685 Feb 12, 2016 (147)
30 ILLUMINA ss1958881433 Feb 12, 2016 (147)
31 JJLAB ss2023626740 Sep 14, 2016 (149)
32 ILLUMINA ss2094822507 Dec 20, 2016 (150)
33 ILLUMINA ss2094952449 Dec 20, 2016 (150)
34 ILLUMINA ss2095174705 Dec 20, 2016 (150)
35 ILLUMINA ss2095174706 Dec 20, 2016 (150)
36 USC_VALOUEV ss2151792027 Nov 08, 2017 (151)
37 HUMAN_LONGEVITY ss2282872996 Dec 20, 2016 (150)
38 TOPMED ss2451242889 Dec 20, 2016 (150)
39 ILLUMINA ss2634424451 Nov 08, 2017 (151)
40 GNOMAD ss2837313615 Nov 08, 2017 (151)
41 AFFY ss2985990657 Nov 08, 2017 (151)
42 SWEGEN ss2998765678 Nov 08, 2017 (151)
43 ILLUMINA ss3022593137 Nov 08, 2017 (151)
44 TOPMED ss3493600122 Nov 08, 2017 (151)
45 ILLUMINA ss3629492534 Oct 12, 2018 (152)
46 ILLUMINA ss3632343646 Oct 12, 2018 (152)
47 ILLUMINA ss3633413394 Oct 12, 2018 (152)
48 ILLUMINA ss3634135718 Oct 12, 2018 (152)
49 ILLUMINA ss3635053756 Oct 12, 2018 (152)
50 ILLUMINA ss3635816839 Oct 12, 2018 (152)
51 ILLUMINA ss3636773610 Oct 12, 2018 (152)
52 ILLUMINA ss3637569599 Oct 12, 2018 (152)
53 ILLUMINA ss3638617160 Oct 12, 2018 (152)
54 ILLUMINA ss3640761052 Oct 12, 2018 (152)
55 ILLUMINA ss3653104162 Oct 12, 2018 (152)
56 1000Genomes NC_000006.11 - 30132625 Oct 12, 2018 (152)
57 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 30132625 Oct 12, 2018 (152)
58 Genetic variation in the Estonian population NC_000006.11 - 30132625 Oct 12, 2018 (152)
59 gnomAD - Genomes NC_000006.11 - 30132625 Oct 12, 2018 (152)
60 TopMed NC_000006.12 - 30164848 Oct 12, 2018 (152)
61 UK 10K study - Twins NC_000006.11 - 30132625 Oct 12, 2018 (152)
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)
rs116116433 May 04, 2012 (137)
rs117531907 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss1592291876, ss1712848627, ss2094952449 NC_000006.10:30240603:G= NC_000006.12:30164847:G= (self)
31277910, 17437600, 12426376, 177941372, 17437600, ss222292064, ss240458912, ss480696398, ss480711969, ss481577808, ss485143022, ss535445556, ss653019000, ss778509864, ss783017802, ss783977849, ss832275270, ss833966096, ss982744503, ss1319512492, ss1581596323, ss1615251155, ss1658245188, ss1752625371, ss1925996685, ss1958881433, ss2023626740, ss2094822507, ss2095174705, ss2095174706, ss2151792027, ss2451242889, ss2634424451, ss2837313615, ss2985990657, ss2998765678, ss3022593137, ss3629492534, ss3632343646, ss3633413394, ss3634135718, ss3635053756, ss3635816839, ss3636773610, ss3637569599, ss3638617160, ss3640761052, ss3653104162 NC_000006.11:30132624:G= NC_000006.12:30164847:G= (self)
334863478, ss2282872996, ss3493600122 NC_000006.12:30164847:G= NC_000006.12:30164847:G= (self)
ss4045325, ss67681233, ss71331297, ss75399948, ss119448400, ss160590835, ss173506305 NT_007592.15:30072624:G= NC_000006.12:30164847:G= (self)
ss1592291876, ss1712848627, ss2094952449 NC_000006.10:30240603:G>A NC_000006.12:30164847:G>A (self)
31277910, 17437600, 12426376, 177941372, 17437600, ss222292064, ss240458912, ss480711969, ss481577808, ss485143022, ss535445556, ss653019000, ss778509864, ss783017802, ss783977849, ss832275270, ss833966096, ss982744503, ss1319512492, ss1581596323, ss1615251155, ss1658245188, ss1752625371, ss1925996685, ss1958881433, ss2023626740, ss2094822507, ss2095174705, ss2095174706, ss2151792027, ss2451242889, ss2634424451, ss2837313615, ss2985990657, ss2998765678, ss3022593137, ss3629492534, ss3632343646, ss3633413394, ss3634135718, ss3635053756, ss3635816839, ss3636773610, ss3637569599, ss3638617160, ss3640761052, ss3653104162 NC_000006.11:30132624:G>A NC_000006.12:30164847:G>A (self)
334863478, ss2282872996, ss3493600122 NC_000006.12:30164847:G>A NC_000006.12:30164847:G>A (self)
ss4045325, ss67681233, ss71331297, ss75399948, ss119448400, ss160590835, ss173506305 NT_007592.15:30072624:G>A NC_000006.12:30164847:G>A (self)
ss480696398 NC_000006.11:30132624:G>C NC_000006.12:30164847:G>C (self)
ss480696398 NC_000006.11:30132624:G>T NC_000006.12:30164847:G>T (self)
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 rs2857449

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.post58+e54ea20