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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.

rs2259594

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr10:132337530 (GRCh38.p13) 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
A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.387514 (102571/264690, TOPMED)
G=0.343874 (84296/245136, GnomAD_exome)
G=0.388919 (54458/140024, GnomAD) (+ 20 more)
G=0.352462 (41477/117678, ExAC)
G=0.39618 (13234/33404, ALFA)
G=0.39481 (6617/16760, 8.3KJPN)
G=0.40135 (5220/13006, GO-ESP)
G=0.3425 (1715/5008, 1000G)
G=0.4123 (1847/4480, Estonian)
G=0.3936 (1517/3854, ALSPAC)
G=0.3975 (1474/3708, TWINSUK)
G=0.3836 (1124/2930, KOREAN)
G=0.3878 (733/1890, HapMap)
G=0.4007 (734/1832, Korea1K)
G=0.411 (410/998, GoNL)
G=0.352 (211/600, NorthernSweden)
G=0.397 (212/534, MGP)
G=0.339 (103/304, FINRISK)
A=0.397 (108/272, SGDP_PRJ)
G=0.407 (88/216, Qatari)
G=0.368 (78/212, Vietnamese)
G=0.38 (15/40, GENOME_DK)
A=0.38 (9/24, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LRRC27 : Intron 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.p13 chr 10 NC_000010.11:g.132337530A>G
GRCh38.p13 chr 10 NC_000010.11:g.132337530A>T
GRCh37.p13 chr 10 NC_000010.10:g.134151034A>G
GRCh37.p13 chr 10 NC_000010.10:g.134151034A>T
Gene: LRRC27, leucine rich repeat containing 27 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LRRC27 transcript variant 2 NM_001143757.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant 3 NM_001143758.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant 4 NM_001143759.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant 5 NM_001309474.2:c.-171-35A…

NM_001309474.2:c.-171-35A>G

N/A Intron Variant
LRRC27 transcript variant 1 NM_030626.3:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X9 XM_006717984.3:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X5 XM_011540208.1:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X7 XM_011540209.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X13 XM_011540210.3:c.-171-35A…

XM_011540210.3:c.-171-35A>G

N/A Intron Variant
LRRC27 transcript variant X8 XM_017016690.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X12 XM_017016691.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X17 XM_017016692.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X18 XM_017016693.2:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X19 XM_024448208.1:c.211-35A>G N/A Intron Variant
LRRC27 transcript variant X20 XM_024448209.1:c.-238-35A…

XM_024448209.1:c.-238-35A>G

N/A Intron Variant
LRRC27 transcript variant X6 XR_001747213.2:n. N/A Intron Variant
LRRC27 transcript variant X1 XR_002957017.1:n. N/A Intron Variant
LRRC27 transcript variant X2 XR_002957018.1:n. N/A Intron Variant
LRRC27 transcript variant X3 XR_002957019.1:n. N/A Intron Variant
LRRC27 transcript variant X4 XR_002957020.1:n. N/A Intron Variant
LRRC27 transcript variant X11 XR_002957021.1:n. N/A Intron Variant
LRRC27 transcript variant X14 XR_002957022.1:n. N/A Intron Variant
LRRC27 transcript variant X15 XR_428718.3:n. N/A Intron Variant
LRRC27 transcript variant X16 XR_428719.2:n. N/A Intron Variant
LRRC27 transcript variant X10 XR_945819.2: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

ALFA Allele Frequency (New)
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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 33404 A=0.60382 G=0.39618
European Sub 24232 A=0.60404 G=0.39596
African Sub 4720 A=0.5794 G=0.4206
African Others Sub 156 A=0.583 G=0.417
African American Sub 4564 A=0.5793 G=0.4207
Asian Sub 180 A=0.667 G=0.333
East Asian Sub 122 A=0.689 G=0.311
Other Asian Sub 58 A=0.62 G=0.38
Latin American 1 Sub 168 A=0.619 G=0.381
Latin American 2 Sub 670 A=0.749 G=0.251
South Asian Sub 98 A=0.80 G=0.20
Other Sub 3336 A=0.5977 G=0.4023


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 264690 A=0.612486 G=0.387514
gnomAD - Exomes Global Study-wide 245136 A=0.656126 G=0.343874
gnomAD - Exomes European Sub 132494 A=0.620956 G=0.379044
gnomAD - Exomes Asian Sub 47800 A=0.71414 G=0.28586
gnomAD - Exomes American Sub 32978 A=0.76672 G=0.23328
gnomAD - Exomes African Sub 16088 A=0.58721 G=0.41279
gnomAD - Exomes Ashkenazi Jewish Sub 9764 A=0.5951 G=0.4049
gnomAD - Exomes Other Sub 6012 A=0.6467 G=0.3533
gnomAD - Genomes Global Study-wide 140024 A=0.611081 G=0.388919
gnomAD - Genomes European Sub 75860 A=0.61674 G=0.38326
gnomAD - Genomes African Sub 41938 A=0.57504 G=0.42496
gnomAD - Genomes American Sub 13638 A=0.68742 G=0.31258
gnomAD - Genomes Ashkenazi Jewish Sub 3318 A=0.5787 G=0.4213
gnomAD - Genomes East Asian Sub 3118 A=0.6430 G=0.3570
gnomAD - Genomes Other Sub 2152 A=0.6338 G=0.3662
ExAC Global Study-wide 117678 A=0.647538 G=0.352462
ExAC Europe Sub 70878 A=0.61200 G=0.38800
ExAC Asian Sub 24466 A=0.71503 G=0.28497
ExAC American Sub 11194 A=0.78337 G=0.21663
ExAC African Sub 10248 A=0.58216 G=0.41784
ExAC Other Sub 892 A=0.667 G=0.333
8.3KJPN JAPANESE Study-wide 16760 A=0.60519 G=0.39481
GO Exome Sequencing Project Global Study-wide 13006 A=0.59865 G=0.40135
GO Exome Sequencing Project European American Sub 8600 A=0.6031 G=0.3969
GO Exome Sequencing Project African American Sub 4406 A=0.5899 G=0.4101
1000Genomes Global Study-wide 5008 A=0.6575 G=0.3425
1000Genomes African Sub 1322 A=0.5885 G=0.4115
1000Genomes East Asian Sub 1008 A=0.6458 G=0.3542
1000Genomes Europe Sub 1006 A=0.6262 G=0.3738
1000Genomes South Asian Sub 978 A=0.744 G=0.256
1000Genomes American Sub 694 A=0.729 G=0.271
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.5877 G=0.4123
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.6064 G=0.3936
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.6025 G=0.3975
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.6164 G=0.3836, T=0.0000
HapMap Global Study-wide 1890 A=0.6122 G=0.3878
HapMap American Sub 768 A=0.663 G=0.337
HapMap African Sub 692 A=0.569 G=0.431
HapMap Asian Sub 254 A=0.626 G=0.374
HapMap Europe Sub 176 A=0.540 G=0.460
Korean Genome Project KOREAN Study-wide 1832 A=0.5993 G=0.4007
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.589 G=0.411
Northern Sweden ACPOP Study-wide 600 A=0.648 G=0.352
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 A=0.603 G=0.397
FINRISK Finnish from FINRISK project Study-wide 304 A=0.661 G=0.339
SGDP_PRJ Global Study-wide 272 A=0.397 G=0.603
Qatari Global Study-wide 216 A=0.593 G=0.407
A Vietnamese Genetic Variation Database Global Study-wide 212 A=0.632 G=0.368
The Danish reference pan genome Danish Study-wide 40 A=0.62 G=0.38
Siberian Global Study-wide 24 A=0.38 G=0.62
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 A= G T
GRCh38.p13 chr 10 NC_000010.11:g.132337530= NC_000010.11:g.132337530A>G NC_000010.11:g.132337530A>T
GRCh37.p13 chr 10 NC_000010.10:g.134151034= NC_000010.10:g.134151034A>G NC_000010.10:g.134151034A>T
LRRC27 transcript variant 2 NM_001143757.1:c.211-35= NM_001143757.1:c.211-35A>G NM_001143757.1:c.211-35A>T
LRRC27 transcript variant 2 NM_001143757.2:c.211-35= NM_001143757.2:c.211-35A>G NM_001143757.2:c.211-35A>T
LRRC27 transcript variant 3 NM_001143758.1:c.211-35= NM_001143758.1:c.211-35A>G NM_001143758.1:c.211-35A>T
LRRC27 transcript variant 3 NM_001143758.2:c.211-35= NM_001143758.2:c.211-35A>G NM_001143758.2:c.211-35A>T
LRRC27 transcript variant 4 NM_001143759.1:c.211-35= NM_001143759.1:c.211-35A>G NM_001143759.1:c.211-35A>T
LRRC27 transcript variant 4 NM_001143759.2:c.211-35= NM_001143759.2:c.211-35A>G NM_001143759.2:c.211-35A>T
LRRC27 transcript variant 5 NM_001309474.2:c.-171-35= NM_001309474.2:c.-171-35A>G NM_001309474.2:c.-171-35A>T
LRRC27 transcript variant 1 NM_030626.2:c.211-35= NM_030626.2:c.211-35A>G NM_030626.2:c.211-35A>T
LRRC27 transcript variant 1 NM_030626.3:c.211-35= NM_030626.3:c.211-35A>G NM_030626.3:c.211-35A>T
LRRC27 transcript variant X9 XM_006717984.3:c.211-35= XM_006717984.3:c.211-35A>G XM_006717984.3:c.211-35A>T
LRRC27 transcript variant X5 XM_011540208.1:c.211-35= XM_011540208.1:c.211-35A>G XM_011540208.1:c.211-35A>T
LRRC27 transcript variant X7 XM_011540209.2:c.211-35= XM_011540209.2:c.211-35A>G XM_011540209.2:c.211-35A>T
LRRC27 transcript variant X13 XM_011540210.3:c.-171-35= XM_011540210.3:c.-171-35A>G XM_011540210.3:c.-171-35A>T
LRRC27 transcript variant X8 XM_017016690.2:c.211-35= XM_017016690.2:c.211-35A>G XM_017016690.2:c.211-35A>T
LRRC27 transcript variant X12 XM_017016691.2:c.211-35= XM_017016691.2:c.211-35A>G XM_017016691.2:c.211-35A>T
LRRC27 transcript variant X17 XM_017016692.2:c.211-35= XM_017016692.2:c.211-35A>G XM_017016692.2:c.211-35A>T
LRRC27 transcript variant X18 XM_017016693.2:c.211-35= XM_017016693.2:c.211-35A>G XM_017016693.2:c.211-35A>T
LRRC27 transcript variant X19 XM_024448208.1:c.211-35= XM_024448208.1:c.211-35A>G XM_024448208.1:c.211-35A>T
LRRC27 transcript variant X20 XM_024448209.1:c.-238-35= XM_024448209.1:c.-238-35A>G XM_024448209.1:c.-238-35A>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#.

82 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 YUSUKE ss3238968 Sep 28, 2001 (100)
2 SC_JCM ss3813556 Sep 28, 2001 (100)
3 BCM_SSAHASNP ss10623491 Jul 11, 2003 (116)
4 ABI ss38524400 Mar 15, 2006 (126)
5 ILLUMINA ss65749638 Oct 14, 2006 (127)
6 ILLUMINA ss74855138 Dec 07, 2007 (129)
7 HUMANGENOME_JCVI ss97698545 Feb 06, 2009 (130)
8 BGI ss102929093 Dec 01, 2009 (131)
9 1000GENOMES ss109890161 Jan 24, 2009 (130)
10 1000GENOMES ss114057896 Jan 25, 2009 (130)
11 ILLUMINA-UK ss119334591 Feb 15, 2009 (130)
12 KRIBB_YJKIM ss119424868 Dec 01, 2009 (131)
13 COMPLETE_GENOMICS ss168821503 Jul 04, 2010 (132)
14 COMPLETE_GENOMICS ss171433689 Jul 04, 2010 (132)
15 ILLUMINA ss173223475 Jul 04, 2010 (132)
16 BUSHMAN ss202231622 Jul 04, 2010 (132)
17 BCM-HGSC-SUB ss207053540 Jul 04, 2010 (132)
18 1000GENOMES ss225036470 Jul 14, 2010 (132)
19 1000GENOMES ss235403843 Jul 15, 2010 (132)
20 1000GENOMES ss242067448 Jul 15, 2010 (132)
21 BL ss254747431 May 09, 2011 (134)
22 GMI ss280841164 May 04, 2012 (137)
23 GMI ss286295242 Apr 25, 2013 (138)
24 PJP ss290969642 May 09, 2011 (134)
25 1000GENOMES ss491007905 May 04, 2012 (137)
26 CLINSEQ_SNP ss491634903 May 04, 2012 (137)
27 ILLUMINA ss535824935 Sep 08, 2015 (146)
28 TISHKOFF ss562318754 Apr 25, 2013 (138)
29 SSMP ss657615425 Apr 25, 2013 (138)
30 NHLBI-ESP ss712982848 Apr 25, 2013 (138)
31 JMKIDD_LAB ss974476855 Aug 21, 2014 (142)
32 EVA-GONL ss988098270 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1067517575 Aug 21, 2014 (142)
34 JMKIDD_LAB ss1077428783 Aug 21, 2014 (142)
35 1000GENOMES ss1339715769 Aug 21, 2014 (142)
36 DDI ss1426498564 Apr 01, 2015 (144)
37 EVA_GENOME_DK ss1575460124 Apr 01, 2015 (144)
38 EVA_FINRISK ss1584071330 Apr 01, 2015 (144)
39 EVA_DECODE ss1597778443 Apr 01, 2015 (144)
40 EVA_UK10K_ALSPAC ss1625792224 Apr 01, 2015 (144)
41 EVA_UK10K_TWINSUK ss1668786257 Apr 01, 2015 (144)
42 EVA_EXAC ss1690140280 Apr 01, 2015 (144)
43 EVA_MGP ss1711275037 Apr 01, 2015 (144)
44 EVA_SVP ss1713225598 Apr 01, 2015 (144)
45 WEILL_CORNELL_DGM ss1931455614 Feb 12, 2016 (147)
46 GENOMED ss1967267449 Jul 19, 2016 (147)
47 JJLAB ss2026469697 Sep 14, 2016 (149)
48 USC_VALOUEV ss2154751058 Dec 20, 2016 (150)
49 HUMAN_LONGEVITY ss2179424896 Dec 20, 2016 (150)
50 TOPMED ss2342539542 Dec 20, 2016 (150)
51 SYSTEMSBIOZJU ss2627704705 Nov 08, 2017 (151)
52 GRF ss2699015841 Nov 08, 2017 (151)
53 GNOMAD ss2738618197 Nov 08, 2017 (151)
54 GNOMAD ss2748500039 Nov 08, 2017 (151)
55 GNOMAD ss2895181365 Nov 08, 2017 (151)
56 SWEGEN ss3007414584 Nov 08, 2017 (151)
57 BIOINF_KMB_FNS_UNIBA ss3027027670 Nov 08, 2017 (151)
58 TOPMED ss3134537994 Nov 08, 2017 (151)
59 CSHL ss3349394592 Nov 08, 2017 (151)
60 ILLUMINA ss3626575229 Oct 12, 2018 (152)
61 ILLUMINA ss3637884246 Oct 12, 2018 (152)
62 ILLUMINA ss3642884605 Oct 12, 2018 (152)
63 OMUKHERJEE_ADBS ss3646417446 Oct 12, 2018 (152)
64 URBANLAB ss3649506005 Oct 12, 2018 (152)
65 EGCUT_WGS ss3674835340 Jul 13, 2019 (153)
66 EVA_DECODE ss3691013878 Jul 13, 2019 (153)
67 ACPOP ss3737826405 Jul 13, 2019 (153)
68 EVA ss3748816897 Jul 13, 2019 (153)
69 KHV_HUMAN_GENOMES ss3814168167 Jul 13, 2019 (153)
70 EVA ss3824568644 Apr 26, 2020 (154)
71 EVA ss3825786846 Apr 26, 2020 (154)
72 EVA ss3832421833 Apr 26, 2020 (154)
73 EVA ss3839753201 Apr 26, 2020 (154)
74 EVA ss3845229213 Apr 26, 2020 (154)
75 SGDP_PRJ ss3875403256 Apr 26, 2020 (154)
76 KRGDB ss3923602070 Apr 26, 2020 (154)
77 KOGIC ss3969004766 Apr 26, 2020 (154)
78 FSA-LAB ss3983989786 Apr 26, 2021 (155)
79 EVA ss3986504391 Apr 26, 2021 (155)
80 EVA ss4017517555 Apr 26, 2021 (155)
81 TOPMED ss4871970628 Apr 26, 2021 (155)
82 TOMMO_GENOMICS ss5200204205 Apr 26, 2021 (155)
83 1000Genomes NC_000010.10 - 134151034 Oct 12, 2018 (152)
84 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 134151034 Oct 12, 2018 (152)
85 Genetic variation in the Estonian population NC_000010.10 - 134151034 Oct 12, 2018 (152)
86 ExAC NC_000010.10 - 134151034 Oct 12, 2018 (152)
87 FINRISK NC_000010.10 - 134151034 Apr 26, 2020 (154)
88 The Danish reference pan genome NC_000010.10 - 134151034 Apr 26, 2020 (154)
89 gnomAD - Genomes NC_000010.11 - 132337530 Apr 26, 2021 (155)
90 gnomAD - Exomes NC_000010.10 - 134151034 Jul 13, 2019 (153)
91 GO Exome Sequencing Project NC_000010.10 - 134151034 Oct 12, 2018 (152)
92 Genome of the Netherlands Release 5 NC_000010.10 - 134151034 Apr 26, 2020 (154)
93 HapMap NC_000010.11 - 132337530 Apr 26, 2020 (154)
94 KOREAN population from KRGDB NC_000010.10 - 134151034 Apr 26, 2020 (154)
95 Korean Genome Project NC_000010.11 - 132337530 Apr 26, 2020 (154)
96 Medical Genome Project healthy controls from Spanish population NC_000010.10 - 134151034 Apr 26, 2020 (154)
97 Northern Sweden NC_000010.10 - 134151034 Jul 13, 2019 (153)
98 Qatari NC_000010.10 - 134151034 Apr 26, 2020 (154)
99 SGDP_PRJ NC_000010.10 - 134151034 Apr 26, 2020 (154)
100 Siberian NC_000010.10 - 134151034 Apr 26, 2020 (154)
101 8.3KJPN NC_000010.10 - 134151034 Apr 26, 2021 (155)
102 TopMed NC_000010.11 - 132337530 Apr 26, 2021 (155)
103 UK 10K study - Twins NC_000010.10 - 134151034 Oct 12, 2018 (152)
104 A Vietnamese Genetic Variation Database NC_000010.10 - 134151034 Jul 13, 2019 (153)
105 ALFA NC_000010.11 - 132337530 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss109890161, ss114057896, ss119334591, ss168821503, ss171433689, ss202231622, ss207053540, ss254747431, ss280841164, ss286295242, ss290969642, ss491634903, ss1597778443, ss1713225598, ss3642884605 NC_000010.9:134001023:A:G NC_000010.11:132337529:A:G (self)
52185046, 28999326, 20573588, 379464, 67791, 2398379, 7823841, 1026303, 12925562, 30779464, 390797, 11111270, 13497544, 27420236, 7267412, 58173512, 28999326, 6437255, ss225036470, ss235403843, ss242067448, ss491007905, ss535824935, ss562318754, ss657615425, ss712982848, ss974476855, ss988098270, ss1067517575, ss1077428783, ss1339715769, ss1426498564, ss1575460124, ss1584071330, ss1625792224, ss1668786257, ss1690140280, ss1711275037, ss1931455614, ss1967267449, ss2026469697, ss2154751058, ss2342539542, ss2627704705, ss2699015841, ss2738618197, ss2748500039, ss2895181365, ss3007414584, ss3349394592, ss3626575229, ss3637884246, ss3646417446, ss3674835340, ss3737826405, ss3748816897, ss3824568644, ss3825786846, ss3832421833, ss3839753201, ss3875403256, ss3923602070, ss3983989786, ss3986504391, ss4017517555, ss5200204205 NC_000010.10:134151033:A:G NC_000010.11:132337529:A:G (self)
368560816, 529492, 25382767, 54971804, 87516283, 14424291054, ss2179424896, ss3027027670, ss3134537994, ss3649506005, ss3691013878, ss3814168167, ss3845229213, ss3969004766, ss4871970628 NC_000010.11:132337529:A:G NC_000010.11:132337529:A:G (self)
ss3238968, ss3813556, ss38524400, ss65749638, ss74855138, ss97698545, ss102929093, ss119424868, ss173223475 NT_008818.16:5384964:A:G NC_000010.11:132337529:A:G (self)
ss10623491 NT_024040.14:423506:A:G NC_000010.11:132337529:A:G (self)
30779464, ss3923602070 NC_000010.10:134151033:A:T NC_000010.11:132337529:A:T (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs2259594

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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
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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.post596+ae089ad