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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.

rs4755797

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:44264337 (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
G=0.315074 (83397/264690, TOPMED)
G=0.286526 (56810/198272, ALFA)
G=0.328132 (45972/140102, GnomAD) (+ 19 more)
G=0.10217 (2887/28258, 14KJPN)
G=0.10229 (1714/16756, 8.3KJPN)
G=0.2523 (1616/6404, 1000G_30x)
G=0.2440 (1222/5008, 1000G)
G=0.3205 (1436/4480, Estonian)
G=0.2600 (1002/3854, ALSPAC)
G=0.2708 (1004/3708, TWINSUK)
G=0.0860 (252/2930, KOREAN)
G=0.2085 (434/2082, HGDP_Stanford)
G=0.3122 (590/1890, HapMap)
G=0.0895 (164/1832, Korea1K)
G=0.272 (271/998, GoNL)
G=0.312 (187/600, NorthernSweden)
G=0.127 (68/534, SGDP_PRJ)
G=0.301 (65/216, Qatari)
G=0.061 (13/212, Vietnamese)
G=0.33 (28/84, Ancient Sardinia)
G=0.21 (10/48, Siberian)
G=0.25 (10/40, GENOME_DK)
Clinical Significance
Reported in ClinVar
Gene : Consequence
ALX4 : 3 Prime UTR 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 198272 G=0.286526 A=0.713474
European Sub 168770 G=0.292576 A=0.707424
African Sub 7086 G=0.4433 A=0.5567
African Others Sub 264 G=0.466 A=0.534
African American Sub 6822 G=0.4424 A=0.5576
Asian Sub 702 G=0.056 A=0.944
East Asian Sub 556 G=0.065 A=0.935
Other Asian Sub 146 G=0.021 A=0.979
Latin American 1 Sub 924 G=0.304 A=0.696
Latin American 2 Sub 8906 G=0.1752 A=0.8248
South Asian Sub 5042 G=0.1081 A=0.8919
Other Sub 6842 G=0.2727 A=0.7273


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=0.315074 A=0.684926
Allele Frequency Aggregator Total Global 198272 G=0.286526 A=0.713474
Allele Frequency Aggregator European Sub 168770 G=0.292576 A=0.707424
Allele Frequency Aggregator Latin American 2 Sub 8906 G=0.1752 A=0.8248
Allele Frequency Aggregator African Sub 7086 G=0.4433 A=0.5567
Allele Frequency Aggregator Other Sub 6842 G=0.2727 A=0.7273
Allele Frequency Aggregator South Asian Sub 5042 G=0.1081 A=0.8919
Allele Frequency Aggregator Latin American 1 Sub 924 G=0.304 A=0.696
Allele Frequency Aggregator Asian Sub 702 G=0.056 A=0.944
gnomAD - Genomes Global Study-wide 140102 G=0.328132 A=0.671868
gnomAD - Genomes European Sub 75884 G=0.29144 A=0.70856
gnomAD - Genomes African Sub 41962 G=0.44760 A=0.55240
gnomAD - Genomes American Sub 13650 G=0.22366 A=0.77634
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.3514 A=0.6486
gnomAD - Genomes East Asian Sub 3130 G=0.0722 A=0.9278
gnomAD - Genomes Other Sub 2152 G=0.2914 A=0.7086
14KJPN JAPANESE Study-wide 28258 G=0.10217 A=0.89783
8.3KJPN JAPANESE Study-wide 16756 G=0.10229 A=0.89771
1000Genomes_30x Global Study-wide 6404 G=0.2523 A=0.7477
1000Genomes_30x African Sub 1786 G=0.4882 A=0.5118
1000Genomes_30x Europe Sub 1266 G=0.3041 A=0.6959
1000Genomes_30x South Asian Sub 1202 G=0.0674 A=0.9326
1000Genomes_30x East Asian Sub 1170 G=0.0718 A=0.9282
1000Genomes_30x American Sub 980 G=0.198 A=0.802
1000Genomes Global Study-wide 5008 G=0.2440 A=0.7560
1000Genomes African Sub 1322 G=0.4849 A=0.5151
1000Genomes East Asian Sub 1008 G=0.0734 A=0.9266
1000Genomes Europe Sub 1006 G=0.3131 A=0.6869
1000Genomes South Asian Sub 978 G=0.059 A=0.941
1000Genomes American Sub 694 G=0.193 A=0.807
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3205 A=0.6795
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.2600 A=0.7400
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.2708 A=0.7292
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0860 A=0.9140
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 G=0.2085 A=0.7915
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.102 A=0.898
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.130 A=0.870
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.346 A=0.654
HGDP-CEPH-db Supplement 1 Europe Sub 318 G=0.314 A=0.686
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.455 A=0.545
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.005 A=0.995
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.00 A=1.00
HapMap Global Study-wide 1890 G=0.3122 A=0.6878
HapMap American Sub 768 G=0.210 A=0.790
HapMap African Sub 692 G=0.494 A=0.506
HapMap Asian Sub 254 G=0.114 A=0.886
HapMap Europe Sub 176 G=0.330 A=0.670
Korean Genome Project KOREAN Study-wide 1832 G=0.0895 A=0.9105
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.272 A=0.728
Northern Sweden ACPOP Study-wide 600 G=0.312 A=0.688
SGDP_PRJ Global Study-wide 534 G=0.127 A=0.873
Qatari Global Study-wide 216 G=0.301 A=0.699
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.061 A=0.939
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 84 G=0.33 A=0.67
Siberian Global Study-wide 48 G=0.21 A=0.79
The Danish reference pan genome Danish Study-wide 40 G=0.25 A=0.75
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 11 NC_000011.10:g.44264337G>A
GRCh37.p13 chr 11 NC_000011.9:g.44285887G>A
ALX4 RefSeqGene (LRG_1256) NG_015809.1:g.50830C>T
Gene: ALX4, ALX homeobox 4 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ALX4 transcript NM_021926.4:c.*517= N/A 3 Prime UTR 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.

Allele: A (allele ID: 320598 )
ClinVar Accession Disease Names Clinical Significance
RCV000264610.3 Parietal foramina 2 Benign
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 11 NC_000011.10:g.44264337= NC_000011.10:g.44264337G>A
GRCh37.p13 chr 11 NC_000011.9:g.44285887= NC_000011.9:g.44285887G>A
ALX4 RefSeqGene (LRG_1256) NG_015809.1:g.50830= NG_015809.1:g.50830C>T
ALX4 transcript NM_021926.4:c.*517= NM_021926.4:c.*517C>T
ALX4 transcript NM_021926.3:c.*517= NM_021926.3:c.*517C>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#.

134 SubSNP, 22 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss6559143 Feb 20, 2003 (111)
2 SC_SNP ss16116251 Feb 27, 2004 (120)
3 CSHL-HAPMAP ss19918347 Feb 27, 2004 (120)
4 SSAHASNP ss20783257 Apr 05, 2004 (121)
5 PERLEGEN ss23603329 Sep 20, 2004 (123)
6 ABI ss38724879 Mar 14, 2006 (126)
7 ILLUMINA ss65743067 Oct 15, 2006 (127)
8 AFFY ss66067406 Nov 30, 2006 (127)
9 ILLUMINA ss67370919 Nov 30, 2006 (127)
10 ILLUMINA ss67753494 Nov 30, 2006 (127)
11 ILLUMINA ss68235475 Dec 12, 2006 (127)
12 PERLEGEN ss69316998 May 17, 2007 (127)
13 ILLUMINA ss70822089 May 26, 2008 (130)
14 ILLUMINA ss71403719 May 17, 2007 (127)
15 ILLUMINA ss75556027 Dec 06, 2007 (129)
16 AFFY ss75993112 Dec 08, 2007 (130)
17 HGSV ss83043853 Dec 16, 2007 (130)
18 HGSV ss83779915 Dec 16, 2007 (130)
19 KRIBB_YJKIM ss84341621 Dec 16, 2007 (130)
20 BCMHGSC_JDW ss88563251 Mar 23, 2008 (129)
21 HUMANGENOME_JCVI ss97383706 Feb 06, 2009 (130)
22 BGI ss102960138 Dec 01, 2009 (131)
23 1000GENOMES ss110425949 Jan 24, 2009 (130)
24 1000GENOMES ss114557794 Jan 25, 2009 (130)
25 ILLUMINA-UK ss119825684 Dec 01, 2009 (131)
26 ENSEMBL ss132472780 Dec 01, 2009 (131)
27 ENSEMBL ss137720106 Dec 01, 2009 (131)
28 ILLUMINA ss154314236 Dec 01, 2009 (131)
29 GMI ss156233933 Dec 01, 2009 (131)
30 ILLUMINA ss159490920 Dec 01, 2009 (131)
31 ILLUMINA ss160707384 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss168308931 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss169809518 Jul 04, 2010 (132)
34 ILLUMINA ss173801249 Jul 04, 2010 (132)
35 COMPLETE_GENOMICS ss175122370 Jul 04, 2010 (132)
36 BUSHMAN ss202659414 Jul 04, 2010 (132)
37 BCM-HGSC-SUB ss207839601 Jul 04, 2010 (132)
38 1000GENOMES ss225226553 Jul 14, 2010 (132)
39 1000GENOMES ss235544124 Jul 15, 2010 (132)
40 1000GENOMES ss242181429 Jul 15, 2010 (132)
41 BL ss255090012 May 09, 2011 (134)
42 GMI ss280984492 May 04, 2012 (137)
43 GMI ss286365673 Apr 25, 2013 (138)
44 PJP ss291233551 May 09, 2011 (134)
45 ILLUMINA ss481033508 May 04, 2012 (137)
46 ILLUMINA ss481054728 May 04, 2012 (137)
47 ILLUMINA ss482043807 Sep 08, 2015 (146)
48 ILLUMINA ss485311773 May 04, 2012 (137)
49 ILLUMINA ss537269111 Sep 08, 2015 (146)
50 TISHKOFF ss562541384 Apr 25, 2013 (138)
51 SSMP ss658035538 Apr 25, 2013 (138)
52 ILLUMINA ss778917745 Sep 08, 2015 (146)
53 ILLUMINA ss783101706 Sep 08, 2015 (146)
54 ILLUMINA ss784058927 Sep 08, 2015 (146)
55 ILLUMINA ss832360281 Sep 08, 2015 (146)
56 ILLUMINA ss833002319 Jul 13, 2019 (153)
57 ILLUMINA ss834379150 Sep 08, 2015 (146)
58 EVA-GONL ss988474202 Aug 21, 2014 (142)
59 JMKIDD_LAB ss1077699376 Aug 21, 2014 (142)
60 1000GENOMES ss1341082440 Aug 21, 2014 (142)
61 DDI ss1426619231 Apr 01, 2015 (144)
62 EVA_GENOME_DK ss1575683279 Apr 01, 2015 (144)
63 EVA_DECODE ss1598150206 Apr 01, 2015 (144)
64 EVA_UK10K_ALSPAC ss1626503554 Apr 01, 2015 (144)
65 EVA_UK10K_TWINSUK ss1669497587 Apr 01, 2015 (144)
66 EVA_SVP ss1713252885 Apr 01, 2015 (144)
67 ILLUMINA ss1752017638 Sep 08, 2015 (146)
68 HAMMER_LAB ss1806804520 Sep 08, 2015 (146)
69 WEILL_CORNELL_DGM ss1931831602 Feb 12, 2016 (147)
70 GENOMED ss1967356996 Jul 19, 2016 (147)
71 JJLAB ss2026663604 Sep 14, 2016 (149)
72 USC_VALOUEV ss2154954498 Dec 20, 2016 (150)
73 HUMAN_LONGEVITY ss2182179198 Dec 20, 2016 (150)
74 SYSTEMSBIOZJU ss2627805900 Nov 08, 2017 (151)
75 ILLUMINA ss2632831571 Nov 08, 2017 (151)
76 GRF ss2699238525 Nov 08, 2017 (151)
77 GNOMAD ss2899041831 Nov 08, 2017 (151)
78 SWEGEN ss3007993193 Nov 08, 2017 (151)
79 BIOINF_KMB_FNS_UNIBA ss3027131314 Nov 08, 2017 (151)
80 CSHL ss3349570760 Nov 08, 2017 (151)
81 ILLUMINA ss3626651632 Oct 12, 2018 (152)
82 ILLUMINA ss3630849131 Oct 12, 2018 (152)
83 ILLUMINA ss3632984841 Oct 12, 2018 (152)
84 ILLUMINA ss3633683908 Oct 12, 2018 (152)
85 ILLUMINA ss3634452073 Oct 12, 2018 (152)
86 ILLUMINA ss3635375594 Oct 12, 2018 (152)
87 ILLUMINA ss3636137143 Oct 12, 2018 (152)
88 ILLUMINA ss3637126421 Oct 12, 2018 (152)
89 ILLUMINA ss3637904638 Oct 12, 2018 (152)
90 ILLUMINA ss3638967774 Oct 12, 2018 (152)
91 ILLUMINA ss3639795140 Oct 12, 2018 (152)
92 ILLUMINA ss3640159412 Oct 12, 2018 (152)
93 ILLUMINA ss3642903252 Oct 12, 2018 (152)
94 ILLUMINA ss3643847300 Oct 12, 2018 (152)
95 OMUKHERJEE_ADBS ss3646424650 Oct 12, 2018 (152)
96 URBANLAB ss3649595773 Oct 12, 2018 (152)
97 EGCUT_WGS ss3675401597 Jul 13, 2019 (153)
98 EVA_DECODE ss3691692874 Jul 13, 2019 (153)
99 ACPOP ss3738140683 Jul 13, 2019 (153)
100 ILLUMINA ss3744752948 Jul 13, 2019 (153)
101 EVA ss3749241777 Jul 13, 2019 (153)
102 ILLUMINA ss3772252969 Jul 13, 2019 (153)
103 PACBIO ss3786941750 Jul 13, 2019 (153)
104 PACBIO ss3792085954 Jul 13, 2019 (153)
105 PACBIO ss3796968174 Jul 13, 2019 (153)
106 KHV_HUMAN_GENOMES ss3814590860 Jul 13, 2019 (153)
107 EVA ss3825796578 Apr 26, 2020 (154)
108 EVA ss3832607472 Apr 26, 2020 (154)
109 EVA ss3839855453 Apr 26, 2020 (154)
110 EVA ss3845333561 Apr 26, 2020 (154)
111 HGDP ss3847417974 Apr 26, 2020 (154)
112 SGDP_PRJ ss3876154035 Apr 26, 2020 (154)
113 KRGDB ss3924422687 Apr 26, 2020 (154)
114 KOGIC ss3969673855 Apr 26, 2020 (154)
115 FSA-LAB ss3984000437 Apr 26, 2021 (155)
116 EVA ss3985533292 Apr 26, 2021 (155)
117 EVA ss3986054510 Apr 26, 2021 (155)
118 EVA ss4017536216 Apr 26, 2021 (155)
119 TOPMED ss4883615459 Apr 26, 2021 (155)
120 TOMMO_GENOMICS ss5201755972 Apr 26, 2021 (155)
121 1000G_HIGH_COVERAGE ss5287241611 Oct 16, 2022 (156)
122 EVA ss5315544997 Oct 16, 2022 (156)
123 EVA ss5399276530 Oct 16, 2022 (156)
124 HUGCELL_USP ss5482460888 Oct 16, 2022 (156)
125 1000G_HIGH_COVERAGE ss5582815215 Oct 16, 2022 (156)
126 SANFORD_IMAGENETICS ss5624274067 Oct 16, 2022 (156)
127 SANFORD_IMAGENETICS ss5651127407 Oct 16, 2022 (156)
128 TOMMO_GENOMICS ss5748812268 Oct 16, 2022 (156)
129 EVA ss5799842208 Oct 16, 2022 (156)
130 YY_MCH ss5812344283 Oct 16, 2022 (156)
131 EVA ss5836595676 Oct 16, 2022 (156)
132 EVA ss5849965236 Oct 16, 2022 (156)
133 EVA ss5919796815 Oct 16, 2022 (156)
134 EVA ss5942444658 Oct 16, 2022 (156)
135 1000Genomes NC_000011.9 - 44285887 Oct 12, 2018 (152)
136 1000Genomes_30x NC_000011.10 - 44264337 Oct 16, 2022 (156)
137 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 44285887 Oct 12, 2018 (152)
138 Genetic variation in the Estonian population NC_000011.9 - 44285887 Oct 12, 2018 (152)
139 The Danish reference pan genome NC_000011.9 - 44285887 Apr 26, 2020 (154)
140 gnomAD - Genomes NC_000011.10 - 44264337 Apr 26, 2021 (155)
141 Genome of the Netherlands Release 5 NC_000011.9 - 44285887 Apr 26, 2020 (154)
142 HGDP-CEPH-db Supplement 1 NC_000011.8 - 44242463 Apr 26, 2020 (154)
143 HapMap NC_000011.10 - 44264337 Apr 26, 2020 (154)
144 KOREAN population from KRGDB NC_000011.9 - 44285887 Apr 26, 2020 (154)
145 Korean Genome Project NC_000011.10 - 44264337 Apr 26, 2020 (154)
146 Northern Sweden NC_000011.9 - 44285887 Jul 13, 2019 (153)
147 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000011.9 - 44285887 Apr 26, 2021 (155)
148 Qatari NC_000011.9 - 44285887 Apr 26, 2020 (154)
149 SGDP_PRJ NC_000011.9 - 44285887 Apr 26, 2020 (154)
150 Siberian NC_000011.9 - 44285887 Apr 26, 2020 (154)
151 8.3KJPN NC_000011.9 - 44285887 Apr 26, 2021 (155)
152 14KJPN NC_000011.10 - 44264337 Oct 16, 2022 (156)
153 TopMed NC_000011.10 - 44264337 Apr 26, 2021 (155)
154 UK 10K study - Twins NC_000011.9 - 44285887 Oct 12, 2018 (152)
155 A Vietnamese Genetic Variation Database NC_000011.9 - 44285887 Jul 13, 2019 (153)
156 ALFA NC_000011.10 - 44264337 Apr 26, 2021 (155)
157 ClinVar RCV000264610.3 Oct 16, 2022 (156)
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)
rs56636549 May 26, 2008 (130)
rs61237253 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
95866, ss83043853, ss83779915, ss88563251, ss110425949, ss114557794, ss119825684, ss168308931, ss169809518, ss175122370, ss202659414, ss207839601, ss255090012, ss280984492, ss286365673, ss291233551, ss481033508, ss1598150206, ss1713252885, ss3638967774, ss3639795140, ss3642903252, ss3643847300, ss3847417974 NC_000011.8:44242462:G:A NC_000011.10:44264336:G:A (self)
53600880, 29780629, 21139845, 2548681, 13286877, 31600081, 11425548, 759219, 13873532, 28171015, 7470852, 59725279, 29780629, 6617705, ss225226553, ss235544124, ss242181429, ss481054728, ss482043807, ss485311773, ss537269111, ss562541384, ss658035538, ss778917745, ss783101706, ss784058927, ss832360281, ss833002319, ss834379150, ss988474202, ss1077699376, ss1341082440, ss1426619231, ss1575683279, ss1626503554, ss1669497587, ss1752017638, ss1806804520, ss1931831602, ss1967356996, ss2026663604, ss2154954498, ss2627805900, ss2632831571, ss2699238525, ss2899041831, ss3007993193, ss3349570760, ss3626651632, ss3630849131, ss3632984841, ss3633683908, ss3634452073, ss3635375594, ss3636137143, ss3637126421, ss3637904638, ss3640159412, ss3646424650, ss3675401597, ss3738140683, ss3744752948, ss3749241777, ss3772252969, ss3786941750, ss3792085954, ss3796968174, ss3825796578, ss3832607472, ss3839855453, ss3876154035, ss3924422687, ss3984000437, ss3985533292, ss3986054510, ss4017536216, ss5201755972, ss5315544997, ss5399276530, ss5624274067, ss5651127407, ss5799842208, ss5836595676, ss5942444658 NC_000011.9:44285886:G:A NC_000011.10:44264336:G:A (self)
RCV000264610.3, 70341150, 378297244, 606419, 26051856, 82649372, 99161115, 7375757296, ss2182179198, ss3027131314, ss3649595773, ss3691692874, ss3814590860, ss3845333561, ss3969673855, ss4883615459, ss5287241611, ss5482460888, ss5582815215, ss5748812268, ss5812344283, ss5849965236, ss5919796815 NC_000011.10:44264336:G:A NC_000011.10:44264336:G:A (self)
ss16116251, ss19918347, ss20783257 NT_009237.16:43049826:G:A NC_000011.10:44264336:G:A (self)
ss6559143, ss23603329, ss38724879, ss65743067, ss66067406, ss67370919, ss67753494, ss68235475, ss69316998, ss70822089, ss71403719, ss75556027, ss75993112, ss84341621, ss97383706, ss102960138, ss132472780, ss137720106, ss154314236, ss156233933, ss159490920, ss160707384, ss173801249 NT_009237.18:44225886:G:A NC_000011.10:44264336: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 rs4755797

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