Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs10105606

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr8:19970337 (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
C>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.339528 (96159/283214, ALFA)
A=0.424500 (112361/264690, TOPMED)
A=0.420344 (58817/139926, GnomAD) (+ 22 more)
A=0.44866 (35308/78696, PAGE_STUDY)
A=0.20089 (3367/16760, 8.3KJPN)
A=0.3926 (1966/5008, 1000G)
A=0.2826 (1266/4480, Estonian)
A=0.3153 (1215/3854, ALSPAC)
A=0.3147 (1167/3708, TWINSUK)
A=0.2089 (612/2930, KOREAN)
A=0.3578 (742/2074, HGDP_Stanford)
A=0.4424 (829/1874, HapMap)
A=0.2036 (373/1832, Korea1K)
A=0.3492 (396/1134, Daghestan)
A=0.308 (307/998, GoNL)
A=0.178 (140/788, PRJEB37584)
A=0.275 (165/600, NorthernSweden)
A=0.006 (3/534, MGP)
C=0.351 (111/316, SGDP_PRJ)
A=0.486 (105/216, Qatari)
A=0.201 (43/214, Vietnamese)
A=0.43 (40/92, Ancient Sardinia)
A=0.23 (9/40, GENOME_DK)
C=0.50 (11/22, Siberian)
A=0.50 (11/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
5 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 8 NC_000008.11:g.19970337C>A
GRCh37.p13 chr 8 NC_000008.10:g.19827848C>A
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
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 283214 C=0.660472 A=0.339528
European Sub 249086 C=0.670359 A=0.329641
African Sub 10176 C=0.34807 A=0.65193
African Others Sub 378 C=0.270 A=0.730
African American Sub 9798 C=0.3511 A=0.6489
Asian Sub 3870 C=0.7853 A=0.2147
East Asian Sub 3138 C=0.7909 A=0.2091
Other Asian Sub 732 C=0.761 A=0.239
Latin American 1 Sub 1040 C=0.6202 A=0.3798
Latin American 2 Sub 6602 C=0.7190 A=0.2810
South Asian Sub 368 C=0.723 A=0.277
Other Sub 12072 C=0.64935 A=0.35065


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 C=0.575500 A=0.424500
gnomAD - Genomes Global Study-wide 139926 C=0.579656 A=0.420344
gnomAD - Genomes European Sub 75824 C=0.68552 A=0.31448
gnomAD - Genomes African Sub 41884 C=0.34600 A=0.65400
gnomAD - Genomes American Sub 13622 C=0.66216 A=0.33784
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.5464 A=0.4536
gnomAD - Genomes East Asian Sub 3124 C=0.8006 A=0.1994
gnomAD - Genomes Other Sub 2150 C=0.6056 A=0.3944
The PAGE Study Global Study-wide 78696 C=0.55134 A=0.44866
The PAGE Study AfricanAmerican Sub 32512 C=0.35442 A=0.64558
The PAGE Study Mexican Sub 10810 C=0.71249 A=0.28751
The PAGE Study Asian Sub 8318 C=0.8082 A=0.1918
The PAGE Study PuertoRican Sub 7918 C=0.5974 A=0.4026
The PAGE Study NativeHawaiian Sub 4534 C=0.8103 A=0.1897
The PAGE Study Cuban Sub 4228 C=0.6081 A=0.3919
The PAGE Study Dominican Sub 3828 C=0.5232 A=0.4768
The PAGE Study CentralAmerican Sub 2450 C=0.6612 A=0.3388
The PAGE Study SouthAmerican Sub 1982 C=0.6948 A=0.3052
The PAGE Study NativeAmerican Sub 1260 C=0.6738 A=0.3262
The PAGE Study SouthAsian Sub 856 C=0.720 A=0.280
8.3KJPN JAPANESE Study-wide 16760 C=0.79911 A=0.20089
1000Genomes Global Study-wide 5008 C=0.6074 A=0.3926
1000Genomes African Sub 1322 C=0.2950 A=0.7050
1000Genomes East Asian Sub 1008 C=0.7659 A=0.2341
1000Genomes Europe Sub 1006 C=0.6561 A=0.3439
1000Genomes South Asian Sub 978 C=0.753 A=0.247
1000Genomes American Sub 694 C=0.697 A=0.303
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.7174 A=0.2826
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.6847 A=0.3153
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.6853 A=0.3147
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.7911 A=0.2089
HGDP-CEPH-db Supplement 1 Global Study-wide 2074 C=0.6422 A=0.3578
HGDP-CEPH-db Supplement 1 Est_Asia Sub 468 C=0.763 A=0.237
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.700 A=0.300
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.591 A=0.409
HGDP-CEPH-db Supplement 1 Europe Sub 318 C=0.594 A=0.406
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.248 A=0.752
HGDP-CEPH-db Supplement 1 America Sub 210 C=0.876 A=0.124
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.62 A=0.38
HapMap Global Study-wide 1874 C=0.5576 A=0.4424
HapMap American Sub 762 C=0.702 A=0.298
HapMap African Sub 686 C=0.290 A=0.710
HapMap Asian Sub 252 C=0.798 A=0.202
HapMap Europe Sub 174 C=0.632 A=0.368
Korean Genome Project KOREAN Study-wide 1832 C=0.7964 A=0.2036
Genome-wide autozygosity in Daghestan Global Study-wide 1134 C=0.6508 A=0.3492
Genome-wide autozygosity in Daghestan Daghestan Sub 626 C=0.649 A=0.351
Genome-wide autozygosity in Daghestan Near_East Sub 144 C=0.632 A=0.368
Genome-wide autozygosity in Daghestan Central Asia Sub 122 C=0.713 A=0.287
Genome-wide autozygosity in Daghestan Europe Sub 108 C=0.639 A=0.361
Genome-wide autozygosity in Daghestan South Asian Sub 98 C=0.62 A=0.38
Genome-wide autozygosity in Daghestan Caucasus Sub 36 C=0.67 A=0.33
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.692 A=0.308
CNV burdens in cranial meningiomas Global Study-wide 788 C=0.822 A=0.178
CNV burdens in cranial meningiomas CRM Sub 788 C=0.822 A=0.178
Northern Sweden ACPOP Study-wide 600 C=0.725 A=0.275
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.994 A=0.006
SGDP_PRJ Global Study-wide 316 C=0.351 A=0.649
Qatari Global Study-wide 216 C=0.514 A=0.486
A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.799 A=0.201
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 92 C=0.57 A=0.43
The Danish reference pan genome Danish Study-wide 40 C=0.78 A=0.23
Siberian Global Study-wide 22 C=0.50 A=0.50
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 C= A
GRCh38.p13 chr 8 NC_000008.11:g.19970337= NC_000008.11:g.19970337C>A
GRCh37.p13 chr 8 NC_000008.10:g.19827848= NC_000008.10:g.19827848C>A
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#.

117 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss13962478 Dec 05, 2003 (119)
2 WI_SSAHASNP ss23033704 Apr 05, 2004 (123)
3 ABI ss43175276 Mar 13, 2006 (126)
4 ILLUMINA ss66869939 Dec 02, 2006 (127)
5 ILLUMINA ss66946296 Dec 02, 2006 (127)
6 ILLUMINA ss68078083 Dec 12, 2006 (127)
7 ILLUMINA ss70465398 May 24, 2008 (130)
8 ILLUMINA ss70986595 May 18, 2007 (127)
9 ILLUMINA ss75528086 Dec 07, 2007 (129)
10 KRIBB_YJKIM ss84905543 Dec 15, 2007 (130)
11 BGI ss104512543 Dec 01, 2009 (131)
12 1000GENOMES ss115099936 Jan 25, 2009 (130)
13 ILLUMINA-UK ss115864276 Feb 14, 2009 (130)
14 ILLUMINA ss159864065 Dec 01, 2009 (131)
15 COMPLETE_GENOMICS ss164131793 Jul 04, 2010 (132)
16 ILLUMINA ss169676931 Jul 04, 2010 (132)
17 BUSHMAN ss198888308 Jul 04, 2010 (132)
18 BCM-HGSC-SUB ss206509197 Jul 04, 2010 (132)
19 1000GENOMES ss223585737 Jul 14, 2010 (132)
20 1000GENOMES ss234352541 Jul 15, 2010 (132)
21 1000GENOMES ss241227351 Jul 15, 2010 (132)
22 BL ss254171597 May 09, 2011 (134)
23 GMI ss279724077 May 04, 2012 (137)
24 GMI ss285808001 Apr 25, 2013 (138)
25 ILLUMINA ss410878623 Sep 17, 2011 (135)
26 ILLUMINA ss479188804 May 04, 2012 (137)
27 ILLUMINA ss479191089 May 04, 2012 (137)
28 ILLUMINA ss479522580 Sep 08, 2015 (146)
29 ILLUMINA ss484395435 May 04, 2012 (137)
30 EXOME_CHIP ss491410906 May 04, 2012 (137)
31 ILLUMINA ss536576831 Sep 08, 2015 (146)
32 TISHKOFF ss560600215 Apr 25, 2013 (138)
33 SSMP ss655035648 Apr 25, 2013 (138)
34 ILLUMINA ss778347408 Sep 08, 2015 (146)
35 ILLUMINA ss782644077 Sep 08, 2015 (146)
36 ILLUMINA ss783613450 Sep 08, 2015 (146)
37 ILLUMINA ss831894321 Sep 08, 2015 (146)
38 ILLUMINA ss833802073 Sep 08, 2015 (146)
39 EVA-GONL ss985272764 Aug 21, 2014 (142)
40 JMKIDD_LAB ss1075340135 Aug 21, 2014 (142)
41 1000GENOMES ss1328915661 Aug 21, 2014 (142)
42 HAMMER_LAB ss1397520223 Sep 08, 2015 (146)
43 DDI ss1431441617 Apr 01, 2015 (144)
44 EVA_GENOME_DK ss1582593823 Apr 01, 2015 (144)
45 EVA_DECODE ss1594862429 Apr 01, 2015 (144)
46 EVA_UK10K_ALSPAC ss1620133994 Apr 01, 2015 (144)
47 EVA_UK10K_TWINSUK ss1663128027 Apr 01, 2015 (144)
48 EVA_MGP ss1711194729 Apr 01, 2015 (144)
49 EVA_SVP ss1713021117 Apr 01, 2015 (144)
50 ILLUMINA ss1752723263 Sep 08, 2015 (146)
51 HAMMER_LAB ss1805432856 Sep 08, 2015 (146)
52 WEILL_CORNELL_DGM ss1928562536 Feb 12, 2016 (147)
53 ILLUMINA ss1946231558 Feb 12, 2016 (147)
54 ILLUMINA ss1959093940 Feb 12, 2016 (147)
55 JJLAB ss2024980635 Sep 14, 2016 (149)
56 USC_VALOUEV ss2153202092 Dec 20, 2016 (150)
57 HUMAN_LONGEVITY ss2301289021 Dec 20, 2016 (150)
58 TOPMED ss2470946912 Dec 20, 2016 (150)
59 SYSTEMSBIOZJU ss2626975190 Nov 08, 2017 (151)
60 ILLUMINA ss2634720499 Nov 08, 2017 (151)
61 ILLUMINA ss2634720500 Nov 08, 2017 (151)
62 ILLUMINA ss2634720501 Nov 08, 2017 (151)
63 GRF ss2708962602 Nov 08, 2017 (151)
64 ILLUMINA ss2711132111 Nov 08, 2017 (151)
65 GNOMAD ss2864094199 Nov 08, 2017 (151)
66 AFFY ss2985433072 Nov 08, 2017 (151)
67 AFFY ss2986076248 Nov 08, 2017 (151)
68 SWEGEN ss3002804618 Nov 08, 2017 (151)
69 ILLUMINA ss3022826135 Nov 08, 2017 (151)
70 BIOINF_KMB_FNS_UNIBA ss3026281158 Nov 08, 2017 (151)
71 CSHL ss3348082094 Nov 08, 2017 (151)
72 TOPMED ss3555885685 Nov 08, 2017 (151)
73 ILLUMINA ss3625947314 Oct 12, 2018 (152)
74 ILLUMINA ss3630013710 Oct 12, 2018 (152)
75 ILLUMINA ss3632621028 Oct 12, 2018 (152)
76 ILLUMINA ss3633493737 Oct 12, 2018 (152)
77 ILLUMINA ss3634220183 Oct 12, 2018 (152)
78 ILLUMINA ss3635162201 Oct 12, 2018 (152)
79 ILLUMINA ss3635899153 Oct 12, 2018 (152)
80 ILLUMINA ss3636899274 Oct 12, 2018 (152)
81 ILLUMINA ss3637652292 Oct 12, 2018 (152)
82 ILLUMINA ss3638748396 Oct 12, 2018 (152)
83 ILLUMINA ss3639376755 Oct 12, 2018 (152)
84 ILLUMINA ss3639983031 Oct 12, 2018 (152)
85 ILLUMINA ss3640869491 Oct 12, 2018 (152)
86 ILLUMINA ss3643680190 Oct 12, 2018 (152)
87 ILLUMINA ss3644026589 Oct 12, 2018 (152)
88 ILLUMINA ss3644964731 Oct 12, 2018 (152)
89 ILLUMINA ss3653367096 Oct 12, 2018 (152)
90 ILLUMINA ss3654194887 Oct 12, 2018 (152)
91 EGCUT_WGS ss3670484673 Jul 13, 2019 (153)
92 EVA_DECODE ss3721555689 Jul 13, 2019 (153)
93 ILLUMINA ss3726520403 Jul 13, 2019 (153)
94 ACPOP ss3735467154 Jul 13, 2019 (153)
95 ILLUMINA ss3744302899 Jul 13, 2019 (153)
96 ILLUMINA ss3744577764 Jul 13, 2019 (153)
97 ILLUMINA ss3745461982 Jul 13, 2019 (153)
98 EVA ss3767717918 Jul 13, 2019 (153)
99 PAGE_CC ss3771428729 Jul 13, 2019 (153)
100 ILLUMINA ss3772954575 Jul 13, 2019 (153)
101 PACBIO ss3786087414 Jul 13, 2019 (153)
102 PACBIO ss3791353817 Jul 13, 2019 (153)
103 PACBIO ss3796234984 Jul 13, 2019 (153)
104 KHV_HUMAN_GENOMES ss3810881405 Jul 13, 2019 (153)
105 EVA ss3831055002 Apr 26, 2020 (154)
106 EVA ss3839037627 Apr 26, 2020 (154)
107 EVA ss3844495651 Apr 26, 2020 (154)
108 HGDP ss3847906874 Apr 26, 2020 (154)
109 SGDP_PRJ ss3869436973 Apr 26, 2020 (154)
110 KRGDB ss3916862805 Apr 26, 2020 (154)
111 KOGIC ss3963402403 Apr 26, 2020 (154)
112 EVA ss3984602272 Apr 27, 2021 (155)
113 EVA ss3985347135 Apr 27, 2021 (155)
114 EVA ss4017379961 Apr 27, 2021 (155)
115 TOPMED ss4778097047 Apr 27, 2021 (155)
116 TOMMO_GENOMICS ss5187654931 Apr 27, 2021 (155)
117 EVA ss5237438130 Apr 27, 2021 (155)
118 1000Genomes NC_000008.10 - 19827848 Oct 12, 2018 (152)
119 The Avon Longitudinal Study of Parents and Children NC_000008.10 - 19827848 Oct 12, 2018 (152)
120 Genome-wide autozygosity in Daghestan NC_000008.9 - 19872128 Apr 26, 2020 (154)
121 Genetic variation in the Estonian population NC_000008.10 - 19827848 Oct 12, 2018 (152)
122 The Danish reference pan genome NC_000008.10 - 19827848 Apr 26, 2020 (154)
123 gnomAD - Genomes NC_000008.11 - 19970337 Apr 27, 2021 (155)
124 Genome of the Netherlands Release 5 NC_000008.10 - 19827848 Apr 26, 2020 (154)
125 HGDP-CEPH-db Supplement 1 NC_000008.9 - 19872128 Apr 26, 2020 (154)
126 HapMap NC_000008.11 - 19970337 Apr 26, 2020 (154)
127 KOREAN population from KRGDB NC_000008.10 - 19827848 Apr 26, 2020 (154)
128 Korean Genome Project NC_000008.11 - 19970337 Apr 26, 2020 (154)
129 Medical Genome Project healthy controls from Spanish population NC_000008.10 - 19827848 Apr 26, 2020 (154)
130 Northern Sweden NC_000008.10 - 19827848 Jul 13, 2019 (153)
131 The PAGE Study NC_000008.11 - 19970337 Jul 13, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000008.10 - 19827848 Apr 27, 2021 (155)
133 CNV burdens in cranial meningiomas NC_000008.10 - 19827848 Apr 27, 2021 (155)
134 Qatari NC_000008.10 - 19827848 Apr 26, 2020 (154)
135 SGDP_PRJ NC_000008.10 - 19827848 Apr 26, 2020 (154)
136 Siberian NC_000008.10 - 19827848 Apr 26, 2020 (154)
137 8.3KJPN NC_000008.10 - 19827848 Apr 27, 2021 (155)
138 TopMed NC_000008.11 - 19970337 Apr 27, 2021 (155)
139 UK 10K study - Twins NC_000008.10 - 19827848 Oct 12, 2018 (152)
140 A Vietnamese Genetic Variation Database NC_000008.10 - 19827848 Jul 13, 2019 (153)
141 ALFA NC_000008.11 - 19970337 Apr 27, 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)
rs13365368 Sep 24, 2004 (123)
rs58654325 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
494117, 584766, ss115099936, ss115864276, ss164131793, ss198888308, ss206509197, ss254171597, ss279724077, ss285808001, ss479188804, ss1397520223, ss1594862429, ss1713021117, ss3639376755, ss3639983031, ss3643680190, ss3644026589, ss3847906874 NC_000008.9:19872127:C:A NC_000008.11:19970336:C:A (self)
41010416, 22797410, 16222921, 8758761, 10187077, 24040199, 310489, 8752019, 573062, 151708, 10604466, 21453953, 5718446, 45624238, 22797410, 5083547, ss223585737, ss234352541, ss241227351, ss479191089, ss479522580, ss484395435, ss491410906, ss536576831, ss560600215, ss655035648, ss778347408, ss782644077, ss783613450, ss831894321, ss833802073, ss985272764, ss1075340135, ss1328915661, ss1431441617, ss1582593823, ss1620133994, ss1663128027, ss1711194729, ss1752723263, ss1805432856, ss1928562536, ss1946231558, ss1959093940, ss2024980635, ss2153202092, ss2470946912, ss2626975190, ss2634720499, ss2634720500, ss2634720501, ss2708962602, ss2711132111, ss2864094199, ss2985433072, ss2986076248, ss3002804618, ss3022826135, ss3348082094, ss3625947314, ss3630013710, ss3632621028, ss3633493737, ss3634220183, ss3635162201, ss3635899153, ss3636899274, ss3637652292, ss3638748396, ss3640869491, ss3644964731, ss3653367096, ss3654194887, ss3670484673, ss3735467154, ss3744302899, ss3744577764, ss3745461982, ss3767717918, ss3772954575, ss3786087414, ss3791353817, ss3796234984, ss3831055002, ss3839037627, ss3869436973, ss3916862805, ss3984602272, ss3985347135, ss4017379961, ss5187654931, ss5237438130 NC_000008.10:19827847:C:A NC_000008.11:19970336:C:A (self)
289198188, 3581043, 19780404, 650198, 384684801, 615474607, 8695415477, ss2301289021, ss3026281158, ss3555885685, ss3721555689, ss3726520403, ss3771428729, ss3810881405, ss3844495651, ss3963402403, ss4778097047 NC_000008.11:19970336:C:A NC_000008.11:19970336:C:A (self)
ss13962478 NT_030737.8:7638768:C:A NC_000008.11:19970336:C:A (self)
ss23033704, ss43175276, ss66869939, ss66946296, ss68078083, ss70465398, ss70986595, ss75528086, ss84905543, ss104512543, ss159864065, ss169676931, ss410878623 NT_167187.1:7685993:C:A NC_000008.11:19970336:C:A (self)
Help

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

5 citations for rs10105606
PMID Title Author Year Journal
19041386 Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review. Boes E et al. 2009 Experimental gerontology
19148283 Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study. Deo RC et al. 2009 PLoS genetics
20864672 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Waterworth DM et al. 2010 Arteriosclerosis, thrombosis, and vascular biology
21995669 A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS. Richardson K et al. 2011 BMC genomics
23832694 Common genetic variants associated with lipid profiles in a Chinese pediatric population. Shen Y et al. 2013 Human genetics
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.post596+ae089ad