Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs10216189

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr7:5485174 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.476905 (126232/264690, TOPMED)
A=0.469715 (66769/142148, ALFA)
A=0.481974 (67431/139906, GnomAD) (+ 19 more)
A=0.49608 (38897/78408, PAGE_STUDY)
G=0.26378 (7454/28258, 14KJPN)
G=0.26399 (4424/16758, 8.3KJPN)
G=0.4756 (3046/6404, 1000G_30x)
G=0.4758 (2383/5008, 1000G)
A=0.4967 (2225/4480, Estonian)
A=0.4598 (1772/3854, ALSPAC)
A=0.4679 (1735/3708, TWINSUK)
G=0.2785 (816/2930, KOREAN)
G=0.4247 (795/1872, HapMap)
A=0.478 (477/998, GoNL)
G=0.317 (248/782, PRJEB37584)
G=0.493 (296/600, NorthernSweden)
G=0.330 (126/382, SGDP_PRJ)
A=0.454 (98/216, Qatari)
G=0.285 (61/214, Vietnamese)
A=0.49 (34/70, Ancient Sardinia)
G=0.40 (16/40, GENOME_DK)
G=0.34 (13/38, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FBXL18 : Intron Variant
LOC124901847 : 2KB Upstream 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 142148 G=0.530285 A=0.469715
European Sub 121698 G=0.525966 A=0.474034
African Sub 6762 G=0.4861 A=0.5139
African Others Sub 234 G=0.453 A=0.547
African American Sub 6528 G=0.4873 A=0.5127
Asian Sub 376 G=0.327 A=0.673
East Asian Sub 276 G=0.315 A=0.685
Other Asian Sub 100 G=0.36 A=0.64
Latin American 1 Sub 720 G=0.476 A=0.524
Latin American 2 Sub 6074 G=0.6874 A=0.3126
South Asian Sub 172 G=0.605 A=0.395
Other Sub 6346 G=0.5260 A=0.4740


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 G=0.523095 A=0.476905
Allele Frequency Aggregator Total Global 142148 G=0.530285 A=0.469715
Allele Frequency Aggregator European Sub 121698 G=0.525966 A=0.474034
Allele Frequency Aggregator African Sub 6762 G=0.4861 A=0.5139
Allele Frequency Aggregator Other Sub 6346 G=0.5260 A=0.4740
Allele Frequency Aggregator Latin American 2 Sub 6074 G=0.6874 A=0.3126
Allele Frequency Aggregator Latin American 1 Sub 720 G=0.476 A=0.524
Allele Frequency Aggregator Asian Sub 376 G=0.327 A=0.673
Allele Frequency Aggregator South Asian Sub 172 G=0.605 A=0.395
gnomAD - Genomes Global Study-wide 139906 G=0.518026 A=0.481974
gnomAD - Genomes European Sub 75774 G=0.52758 A=0.47242
gnomAD - Genomes African Sub 41926 G=0.48736 A=0.51264
gnomAD - Genomes American Sub 13616 G=0.59702 A=0.40298
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.5656 A=0.4344
gnomAD - Genomes East Asian Sub 3116 G=0.3129 A=0.6871
gnomAD - Genomes Other Sub 2150 G=0.5028 A=0.4972
The PAGE Study Global Study-wide 78408 G=0.50392 A=0.49608
The PAGE Study AfricanAmerican Sub 32386 G=0.48722 A=0.51278
The PAGE Study Mexican Sub 10776 G=0.68940 A=0.31060
The PAGE Study Asian Sub 8278 G=0.2799 A=0.7201
The PAGE Study PuertoRican Sub 7900 G=0.5042 A=0.4958
The PAGE Study NativeHawaiian Sub 4512 G=0.3617 A=0.6383
The PAGE Study Cuban Sub 4218 G=0.5429 A=0.4571
The PAGE Study Dominican Sub 3816 G=0.5280 A=0.4720
The PAGE Study CentralAmerican Sub 2442 G=0.6581 A=0.3419
The PAGE Study SouthAmerican Sub 1970 G=0.6487 A=0.3513
The PAGE Study NativeAmerican Sub 1258 G=0.5644 A=0.4356
The PAGE Study SouthAsian Sub 852 G=0.553 A=0.447
14KJPN JAPANESE Study-wide 28258 G=0.26378 A=0.73622
8.3KJPN JAPANESE Study-wide 16758 G=0.26399 A=0.73601
1000Genomes_30x Global Study-wide 6404 G=0.4756 A=0.5244
1000Genomes_30x African Sub 1786 G=0.4748 A=0.5252
1000Genomes_30x Europe Sub 1266 G=0.4834 A=0.5166
1000Genomes_30x South Asian Sub 1202 G=0.5433 A=0.4567
1000Genomes_30x East Asian Sub 1170 G=0.2846 A=0.7154
1000Genomes_30x American Sub 980 G=0.612 A=0.388
1000Genomes Global Study-wide 5008 G=0.4758 A=0.5242
1000Genomes African Sub 1322 G=0.4750 A=0.5250
1000Genomes East Asian Sub 1008 G=0.2946 A=0.7054
1000Genomes Europe Sub 1006 G=0.4891 A=0.5109
1000Genomes South Asian Sub 978 G=0.550 A=0.450
1000Genomes American Sub 694 G=0.617 A=0.383
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.5033 A=0.4967
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.5402 A=0.4598
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.5321 A=0.4679
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.2785 A=0.7215
HapMap Global Study-wide 1872 G=0.4247 A=0.5753
HapMap American Sub 770 G=0.451 A=0.549
HapMap African Sub 678 G=0.437 A=0.563
HapMap Asian Sub 254 G=0.252 A=0.748
HapMap Europe Sub 170 G=0.518 A=0.482
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.522 A=0.478
CNV burdens in cranial meningiomas Global Study-wide 782 G=0.317 A=0.683
CNV burdens in cranial meningiomas CRM Sub 782 G=0.317 A=0.683
Northern Sweden ACPOP Study-wide 600 G=0.493 A=0.507
SGDP_PRJ Global Study-wide 382 G=0.330 A=0.670
Qatari Global Study-wide 216 G=0.546 A=0.454
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.285 A=0.715
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 70 G=0.51 A=0.49
The Danish reference pan genome Danish Study-wide 40 G=0.40 A=0.60
Siberian Global Study-wide 38 G=0.34 A=0.66
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 7 NC_000007.14:g.5485174G>A
GRCh37.p13 chr 7 NC_000007.13:g.5524805G>A
Gene: FBXL18, F-box and leucine rich repeat protein 18 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
FBXL18 transcript variant 3 NM_001363441.2:c.2000+605…

NM_001363441.2:c.2000+6057C>T

 		N/A Intron Variant
FBXL18 transcript variant 5 NM_001367780.1:c.1701-324…

NM_001367780.1:c.1701-3243C>T

 		N/A Intron Variant
FBXL18 transcript variant 6 NM_001367781.1:c.1701-324…

NM_001367781.1:c.1701-3243C>T

 		N/A Intron Variant
FBXL18 transcript variant 2 NM_024963.6:c.2001-3243C>T N/A Intron Variant
FBXL18 transcript variant 1 NM_001321213.2:c. N/A Genic Downstream Transcript Variant
FBXL18 transcript variant 4 NM_001363442.2:c. N/A Genic Downstream Transcript Variant
Gene: LOC124901847, uncharacterized LOC124901847 (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
LOC124901847 transcript XR_007060681.1:n. 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

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
GRCh38.p14 chr 7 NC_000007.14:g.5485174= NC_000007.14:g.5485174G>A
GRCh37.p13 chr 7 NC_000007.13:g.5524805= NC_000007.13:g.5524805G>A
FBXL18 transcript variant 3 NM_001363441.2:c.2000+6057= NM_001363441.2:c.2000+6057C>T
FBXL18 transcript variant 5 NM_001367780.1:c.1701-3243= NM_001367780.1:c.1701-3243C>T
FBXL18 transcript variant 6 NM_001367781.1:c.1701-3243= NM_001367781.1:c.1701-3243C>T
FBXL18 transcript NM_024963.4:c.2001-3243= NM_024963.4:c.2001-3243C>T
FBXL18 transcript variant 2 NM_024963.6:c.2001-3243= NM_024963.6:c.2001-3243C>T
FBXL18 transcript variant X2 XM_005249854.1:c.2001-3250= XM_005249854.1:c.2001-3250C>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#.

118 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 WUGSC_SSAHASNP ss14083105 Dec 05, 2003 (119)
2 PERLEGEN ss69003017 May 16, 2007 (127)
3 ILLUMINA ss75106195 Dec 07, 2007 (129)
4 HGSV ss78875944 Dec 07, 2007 (129)
5 HGSV ss82811699 Dec 15, 2007 (130)
6 BCMHGSC_JDW ss93618279 Mar 24, 2008 (129)
7 BGI ss104393474 Dec 01, 2009 (131)
8 1000GENOMES ss111436283 Jan 25, 2009 (130)
9 1000GENOMES ss113226505 Jan 25, 2009 (130)
10 ILLUMINA-UK ss115901156 Feb 14, 2009 (130)
11 KRIBB_YJKIM ss119617456 Dec 01, 2009 (131)
12 ENSEMBL ss142599288 Dec 01, 2009 (131)
13 GMI ss157980388 Dec 01, 2009 (131)
14 ILLUMINA ss159879009 Dec 01, 2009 (131)
15 COMPLETE_GENOMICS ss162001200 Jul 04, 2010 (132)
16 COMPLETE_GENOMICS ss163572547 Jul 04, 2010 (132)
17 ILLUMINA ss169868668 Jul 04, 2010 (132)
18 BUSHMAN ss202868697 Jul 04, 2010 (132)
19 BCM-HGSC-SUB ss208422595 Jul 04, 2010 (132)
20 1000GENOMES ss222873207 Jul 14, 2010 (132)
21 1000GENOMES ss233824615 Jul 15, 2010 (132)
22 1000GENOMES ss240810523 Jul 15, 2010 (132)
23 BL ss254009481 May 09, 2011 (134)
24 GMI ss279160253 May 04, 2012 (137)
25 GMI ss285564550 Apr 25, 2013 (138)
26 PJP ss293920265 May 09, 2011 (134)
27 ILLUMINA ss479227159 May 04, 2012 (137)
28 ILLUMINA ss479229632 May 04, 2012 (137)
29 ILLUMINA ss479582123 Sep 08, 2015 (146)
30 ILLUMINA ss484414368 May 04, 2012 (137)
31 ILLUMINA ss536590753 Sep 08, 2015 (146)
32 TISHKOFF ss559767086 Apr 25, 2013 (138)
33 SSMP ss654114069 Apr 25, 2013 (138)
34 ILLUMINA ss779026464 Sep 08, 2015 (146)
35 ILLUMINA ss782653615 Sep 08, 2015 (146)
36 ILLUMINA ss783622793 Sep 08, 2015 (146)
37 ILLUMINA ss831903981 Sep 08, 2015 (146)
38 ILLUMINA ss834489121 Sep 08, 2015 (146)
39 EVA-GONL ss983881619 Aug 21, 2014 (142)
40 JMKIDD_LAB ss1074311115 Aug 21, 2014 (142)
41 1000GENOMES ss1323692811 Aug 21, 2014 (142)
42 DDI ss1431007348 Apr 01, 2015 (144)
43 EVA_GENOME_DK ss1582043677 Apr 01, 2015 (144)
44 EVA_DECODE ss1593447354 Apr 01, 2015 (144)
45 EVA_UK10K_ALSPAC ss1617451127 Apr 01, 2015 (144)
46 EVA_UK10K_TWINSUK ss1660445160 Apr 01, 2015 (144)
47 EVA_SVP ss1712926698 Apr 01, 2015 (144)
48 ILLUMINA ss1752690732 Sep 08, 2015 (146)
49 HAMMER_LAB ss1804838970 Sep 08, 2015 (146)
50 WEILL_CORNELL_DGM ss1927126008 Feb 12, 2016 (147)
51 ILLUMINA ss1958983244 Feb 12, 2016 (147)
52 GENOMED ss1970608575 Jul 19, 2016 (147)
53 JJLAB ss2024232631 Sep 14, 2016 (149)
54 USC_VALOUEV ss2152432545 Dec 20, 2016 (150)
55 HUMAN_LONGEVITY ss2291290636 Dec 20, 2016 (150)
56 SYSTEMSBIOZJU ss2626606081 Nov 08, 2017 (151)
57 ILLUMINA ss2634558651 Nov 08, 2017 (151)
58 GRF ss2708080865 Nov 08, 2017 (151)
59 GNOMAD ss2849102536 Nov 08, 2017 (151)
60 AFFY ss2986028555 Nov 08, 2017 (151)
61 SWEGEN ss3000528378 Nov 08, 2017 (151)
62 ILLUMINA ss3022702631 Nov 08, 2017 (151)
63 BIOINF_KMB_FNS_UNIBA ss3025910761 Nov 08, 2017 (151)
64 CSHL ss3347405733 Nov 08, 2017 (151)
65 ILLUMINA ss3625920732 Oct 12, 2018 (152)
66 ILLUMINA ss3629738271 Oct 12, 2018 (152)
67 ILLUMINA ss3632468892 Oct 12, 2018 (152)
68 ILLUMINA ss3634174304 Oct 12, 2018 (152)
69 ILLUMINA ss3635105073 Oct 12, 2018 (152)
70 ILLUMINA ss3635854431 Oct 12, 2018 (152)
71 ILLUMINA ss3636834610 Oct 12, 2018 (152)
72 ILLUMINA ss3637607375 Oct 12, 2018 (152)
73 ILLUMINA ss3638676858 Oct 12, 2018 (152)
74 ILLUMINA ss3640812374 Oct 12, 2018 (152)
75 ILLUMINA ss3641207224 Oct 12, 2018 (152)
76 ILLUMINA ss3641504581 Oct 12, 2018 (152)
77 ILLUMINA ss3643614562 Oct 12, 2018 (152)
78 ILLUMINA ss3644933766 Oct 12, 2018 (152)
79 ILLUMINA ss3653229812 Oct 12, 2018 (152)
80 EGCUT_WGS ss3668455776 Jul 13, 2019 (153)
81 EVA_DECODE ss3718986009 Jul 13, 2019 (153)
82 ILLUMINA ss3726415420 Jul 13, 2019 (153)
83 ACPOP ss3734302284 Jul 13, 2019 (153)
84 ILLUMINA ss3745404974 Jul 13, 2019 (153)
85 EVA ss3766117066 Jul 13, 2019 (153)
86 PAGE_CC ss3771347518 Jul 13, 2019 (153)
87 ILLUMINA ss3772898211 Jul 13, 2019 (153)
88 PACBIO ss3785717244 Jul 13, 2019 (153)
89 PACBIO ss3791033306 Jul 13, 2019 (153)
90 PACBIO ss3795913006 Jul 13, 2019 (153)
91 KHV_HUMAN_GENOMES ss3809278641 Jul 13, 2019 (153)
92 EVA ss3830380372 Apr 26, 2020 (154)
93 EVA ss3838677008 Apr 26, 2020 (154)
94 EVA ss3844127449 Apr 26, 2020 (154)
95 SGDP_PRJ ss3866498750 Apr 26, 2020 (154)
96 KRGDB ss3913520333 Apr 26, 2020 (154)
97 EVA ss3984582415 Apr 26, 2021 (155)
98 EVA ss3985273999 Apr 26, 2021 (155)
99 EVA ss4017317436 Apr 26, 2021 (155)
100 TOPMED ss4733618619 Apr 26, 2021 (155)
101 TOMMO_GENOMICS ss5181552041 Apr 26, 2021 (155)
102 1000G_HIGH_COVERAGE ss5271617627 Oct 14, 2022 (156)
103 EVA ss5315218824 Oct 14, 2022 (156)
104 EVA ss5371286643 Oct 14, 2022 (156)
105 HUGCELL_USP ss5468929728 Oct 14, 2022 (156)
106 EVA ss5508827969 Oct 14, 2022 (156)
107 1000G_HIGH_COVERAGE ss5559153083 Oct 14, 2022 (156)
108 SANFORD_IMAGENETICS ss5624652819 Oct 14, 2022 (156)
109 SANFORD_IMAGENETICS ss5642217677 Oct 14, 2022 (156)
110 TOMMO_GENOMICS ss5720931505 Oct 14, 2022 (156)
111 EVA ss5799713293 Oct 14, 2022 (156)
112 YY_MCH ss5808279941 Oct 14, 2022 (156)
113 EVA ss5822325764 Oct 14, 2022 (156)
114 EVA ss5848126492 Oct 14, 2022 (156)
115 EVA ss5855735801 Oct 14, 2022 (156)
116 EVA ss5857474288 Oct 14, 2022 (156)
117 EVA ss5971409792 Oct 14, 2022 (156)
118 EVA ss5980414262 Oct 14, 2022 (156)
119 1000Genomes NC_000007.13 - 5524805 Oct 12, 2018 (152)
120 1000Genomes_30x NC_000007.14 - 5485174 Oct 14, 2022 (156)
121 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 5524805 Oct 12, 2018 (152)
122 Genetic variation in the Estonian population NC_000007.13 - 5524805 Oct 12, 2018 (152)
123 The Danish reference pan genome NC_000007.13 - 5524805 Apr 26, 2020 (154)
124 gnomAD - Genomes NC_000007.14 - 5485174 Apr 26, 2021 (155)
125 Genome of the Netherlands Release 5 NC_000007.13 - 5524805 Apr 26, 2020 (154)
126 HapMap NC_000007.14 - 5485174 Apr 26, 2020 (154)
127 KOREAN population from KRGDB NC_000007.13 - 5524805 Apr 26, 2020 (154)
128 Northern Sweden NC_000007.13 - 5524805 Jul 13, 2019 (153)
129 The PAGE Study NC_000007.14 - 5485174 Jul 13, 2019 (153)
130 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 5524805 Apr 26, 2021 (155)
131 CNV burdens in cranial meningiomas NC_000007.13 - 5524805 Apr 26, 2021 (155)
132 Qatari NC_000007.13 - 5524805 Apr 26, 2020 (154)
133 SGDP_PRJ NC_000007.13 - 5524805 Apr 26, 2020 (154)
134 Siberian NC_000007.13 - 5524805 Apr 26, 2020 (154)
135 8.3KJPN NC_000007.13 - 5524805 Apr 26, 2021 (155)
136 14KJPN NC_000007.14 - 5485174 Oct 14, 2022 (156)
137 TopMed NC_000007.14 - 5485174 Apr 26, 2021 (155)
138 UK 10K study - Twins NC_000007.13 - 5524805 Oct 12, 2018 (152)
139 A Vietnamese Genetic Variation Database NC_000007.13 - 5524805 Jul 13, 2019 (153)
140 ALFA NC_000007.14 - 5485174 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)
rs58508307 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78875944, ss82811699 NC_000007.11:5298045:G:A NC_000007.14:5485173:G:A (self)
ss93618279, ss111436283, ss113226505, ss115901156, ss162001200, ss163572547, ss202868697, ss208422595, ss254009481, ss279160253, ss285564550, ss293920265, ss479227159, ss1593447354, ss1712926698, ss3643614562 NC_000007.12:5491330:G:A NC_000007.14:5485173:G:A (self)
35612978, 19855886, 14194024, 8208616, 8842123, 20697727, 7587149, 499926, 131834, 9167938, 18515730, 4948899, 39521348, 19855886, 4419534, ss222873207, ss233824615, ss240810523, ss479229632, ss479582123, ss484414368, ss536590753, ss559767086, ss654114069, ss779026464, ss782653615, ss783622793, ss831903981, ss834489121, ss983881619, ss1074311115, ss1323692811, ss1431007348, ss1582043677, ss1617451127, ss1660445160, ss1752690732, ss1804838970, ss1927126008, ss1958983244, ss1970608575, ss2024232631, ss2152432545, ss2626606081, ss2634558651, ss2708080865, ss2849102536, ss2986028555, ss3000528378, ss3022702631, ss3347405733, ss3625920732, ss3629738271, ss3632468892, ss3634174304, ss3635105073, ss3635854431, ss3636834610, ss3637607375, ss3638676858, ss3640812374, ss3641207224, ss3641504581, ss3644933766, ss3653229812, ss3668455776, ss3734302284, ss3745404974, ss3766117066, ss3772898211, ss3785717244, ss3791033306, ss3795913006, ss3830380372, ss3838677008, ss3866498750, ss3913520333, ss3984582415, ss3985273999, ss4017317436, ss5181552041, ss5315218824, ss5371286643, ss5508827969, ss5624652819, ss5642217677, ss5799713293, ss5822325764, ss5848126492, ss5971409792, ss5980414262 NC_000007.13:5524804:G:A NC_000007.14:5485173:G:A (self)
46679018, 251219925, 3322432, 568987, 54768609, 570996178, 3871259965, ss2291290636, ss3025910761, ss3718986009, ss3726415420, ss3771347518, ss3809278641, ss3844127449, ss4733618619, ss5271617627, ss5468929728, ss5559153083, ss5720931505, ss5808279941, ss5855735801, ss5857474288 NC_000007.14:5485173:G:A NC_000007.14:5485173:G:A (self)
ss14083105 NT_007819.14:4820478:G:A NC_000007.14:5485173:G:A (self)
ss69003017, ss75106195, ss104393474, ss119617456, ss142599288, ss157980388, ss159879009, ss169868668 NT_007819.17:5514804:G:A NC_000007.14:5485173:G:A (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 rs10216189

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.post761+d5e8e07