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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.

rs5049

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:230714337 (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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.162900 (43118/264690, TOPMED)
T=0.161225 (22585/140084, GnomAD)
T=0.18694 (14706/78666, PAGE_STUDY) (+ 20 more)
T=0.16251 (4592/28256, 14KJPN)
T=0.14912 (2960/19850, ALFA)
T=0.16474 (2761/16760, 8.3KJPN)
T=0.1860 (1191/6404, 1000G_30x)
T=0.1895 (949/5008, 1000G)
T=0.1357 (608/4480, Estonian)
T=0.1079 (416/3854, ALSPAC)
T=0.1092 (405/3708, TWINSUK)
T=0.1819 (533/2930, KOREAN)
T=0.2036 (373/1832, Korea1K)
T=0.094 (94/998, GoNL)
T=0.162 (128/790, PRJEB37584)
T=0.105 (63/600, NorthernSweden)
T=0.185 (40/216, Qatari)
T=0.213 (46/216, Vietnamese)
C=0.443 (70/158, SGDP_PRJ)
T=0.18 (16/88, PharmGKB)
T=0.03 (1/40, GENOME_DK)
C=0.50 (7/14, Siberian)
T=0.50 (7/14, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
AGT : Intron Variant
Publications
10 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 19850 C=0.85088 T=0.14912
European Sub 14364 C=0.87622 T=0.12378
African Sub 3404 C=0.7382 T=0.2618
African Others Sub 114 C=0.728 T=0.272
African American Sub 3290 C=0.7386 T=0.2614
Asian Sub 150 C=0.820 T=0.180
East Asian Sub 122 C=0.811 T=0.189
Other Asian Sub 28 C=0.86 T=0.14
Latin American 1 Sub 154 C=0.844 T=0.156
Latin American 2 Sub 616 C=0.903 T=0.097
South Asian Sub 104 C=0.808 T=0.192
Other Sub 1058 C=0.8488 T=0.1512


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=0.837100 T=0.162900
gnomAD - Genomes Global Study-wide 140084 C=0.838775 T=0.161225
gnomAD - Genomes European Sub 75912 C=0.88771 T=0.11229
gnomAD - Genomes African Sub 41930 C=0.73453 T=0.26547
gnomAD - Genomes American Sub 13646 C=0.86817 T=0.13183
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.9143 T=0.0857
gnomAD - Genomes East Asian Sub 3126 C=0.8221 T=0.1779
gnomAD - Genomes Other Sub 2146 C=0.8649 T=0.1351
The PAGE Study Global Study-wide 78666 C=0.81306 T=0.18694
The PAGE Study AfricanAmerican Sub 32492 C=0.73975 T=0.26025
The PAGE Study Mexican Sub 10806 C=0.90912 T=0.09088
The PAGE Study Asian Sub 8314 C=0.8328 T=0.1672
The PAGE Study PuertoRican Sub 7916 C=0.8426 T=0.1574
The PAGE Study NativeHawaiian Sub 4534 C=0.8703 T=0.1297
The PAGE Study Cuban Sub 4230 C=0.8809 T=0.1191
The PAGE Study Dominican Sub 3826 C=0.8254 T=0.1746
The PAGE Study CentralAmerican Sub 2450 C=0.8767 T=0.1233
The PAGE Study SouthAmerican Sub 1982 C=0.8996 T=0.1004
The PAGE Study NativeAmerican Sub 1260 C=0.8532 T=0.1468
The PAGE Study SouthAsian Sub 856 C=0.783 T=0.217
14KJPN JAPANESE Study-wide 28256 C=0.83749 T=0.16251
Allele Frequency Aggregator Total Global 19850 C=0.85088 T=0.14912
Allele Frequency Aggregator European Sub 14364 C=0.87622 T=0.12378
Allele Frequency Aggregator African Sub 3404 C=0.7382 T=0.2618
Allele Frequency Aggregator Other Sub 1058 C=0.8488 T=0.1512
Allele Frequency Aggregator Latin American 2 Sub 616 C=0.903 T=0.097
Allele Frequency Aggregator Latin American 1 Sub 154 C=0.844 T=0.156
Allele Frequency Aggregator Asian Sub 150 C=0.820 T=0.180
Allele Frequency Aggregator South Asian Sub 104 C=0.808 T=0.192
8.3KJPN JAPANESE Study-wide 16760 C=0.83526 T=0.16474
1000Genomes_30x Global Study-wide 6404 C=0.8140 T=0.1860
1000Genomes_30x African Sub 1786 C=0.7184 T=0.2816
1000Genomes_30x Europe Sub 1266 C=0.8989 T=0.1011
1000Genomes_30x South Asian Sub 1202 C=0.7820 T=0.2180
1000Genomes_30x East Asian Sub 1170 C=0.8222 T=0.1778
1000Genomes_30x American Sub 980 C=0.908 T=0.092
1000Genomes Global Study-wide 5008 C=0.8105 T=0.1895
1000Genomes African Sub 1322 C=0.7088 T=0.2912
1000Genomes East Asian Sub 1008 C=0.8214 T=0.1786
1000Genomes Europe Sub 1006 C=0.8946 T=0.1054
1000Genomes South Asian Sub 978 C=0.780 T=0.220
1000Genomes American Sub 694 C=0.909 T=0.091
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.8643 T=0.1357
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.8921 T=0.1079
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.8908 T=0.1092
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.8181 T=0.1819
Korean Genome Project KOREAN Study-wide 1832 C=0.7964 T=0.2036
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.906 T=0.094
CNV burdens in cranial meningiomas Global Study-wide 790 C=0.838 T=0.162
CNV burdens in cranial meningiomas CRM Sub 790 C=0.838 T=0.162
Northern Sweden ACPOP Study-wide 600 C=0.895 T=0.105
Qatari Global Study-wide 216 C=0.815 T=0.185
A Vietnamese Genetic Variation Database Global Study-wide 216 C=0.787 T=0.213
SGDP_PRJ Global Study-wide 158 C=0.443 T=0.557
PharmGKB Aggregated Global Study-wide 88 C=0.82 T=0.18
PharmGKB Aggregated PA151490457 Sub 88 C=0.82 T=0.18
The Danish reference pan genome Danish Study-wide 40 C=0.97 T=0.03
Siberian Global Study-wide 14 C=0.50 T=0.50
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 1 NC_000001.11:g.230714337C>T
GRCh37.p13 chr 1 NC_000001.10:g.230850083C>T
AGT RefSeqGene NG_008836.2:g.5254G>A
Gene: AGT, angiotensinogen (minus strand)
Molecule type Change Amino acid[Codon] SO Term
AGT transcript variant 2 NM_001382817.3:c.-30-3484…

NM_001382817.3:c.-30-3484G>A

N/A Intron Variant
AGT transcript variant 1 NM_001384479.1:c. N/A Genic 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.

Allele: T (allele ID: 279450 )
ClinVar Accession Disease Names Clinical Significance
RCV000343947.5 Renal tubular dysgenesis Benign
RCV001723880.3 not provided 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 C= T
GRCh38.p14 chr 1 NC_000001.11:g.230714337= NC_000001.11:g.230714337C>T
GRCh37.p13 chr 1 NC_000001.10:g.230850083= NC_000001.10:g.230850083C>T
AGT RefSeqGene NG_008836.2:g.5254= NG_008836.2:g.5254G>A
AGT transcript NM_000029.3:c.-255= NM_000029.3:c.-255G>A
AGT transcript variant 2 NM_001382817.3:c.-30-3484= NM_001382817.3:c.-30-3484G>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#.

85 SubSNP, 22 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 ARAVINDA ss6493 Sep 19, 2000 (52)
2 WI_SSAHASNP ss6695690 Feb 20, 2003 (111)
3 PARC ss16338931 Feb 27, 2004 (120)
4 IMCJ-GDT ss22886634 Apr 05, 2004 (121)
5 PERLEGEN ss23235290 Sep 20, 2004 (123)
6 KYUGEN ss28460762 Sep 20, 2004 (123)
7 SSAHASNP ss35217928 May 24, 2005 (125)
8 STEJUSTINE-REGGEN ss51853114 Mar 16, 2006 (126)
9 PHARMGKB_PARC ss84151187 Dec 14, 2007 (130)
10 RSG_UW ss86211278 Mar 23, 2008 (129)
11 RSG_JCVI ss86215615 Mar 23, 2008 (129)
12 KRIBB_YJKIM ss102649989 Feb 04, 2009 (130)
13 1000GENOMES ss109021241 Jan 23, 2009 (130)
14 1000GENOMES ss111914277 Jan 25, 2009 (130)
15 ILLUMINA-UK ss119241052 Feb 15, 2009 (130)
16 GMI ss156402080 Dec 01, 2009 (131)
17 COMPLETE_GENOMICS ss165369105 Jul 04, 2010 (132)
18 BUSHMAN ss199729384 Jul 04, 2010 (132)
19 1000GENOMES ss218933442 Jul 14, 2010 (132)
20 1000GENOMES ss230940984 Jul 14, 2010 (132)
21 1000GENOMES ss238547539 Jul 15, 2010 (132)
22 ILLUMINA ss244302762 Jul 04, 2010 (132)
23 GMI ss276256148 May 04, 2012 (137)
24 ILLUMINA ss532918253 Sep 08, 2015 (146)
25 TISHKOFF ss555199779 Apr 25, 2013 (138)
26 SSMP ss648772964 Apr 25, 2013 (138)
27 EVA-GONL ss976246049 Aug 21, 2014 (142)
28 JMKIDD_LAB ss1068678347 Aug 21, 2014 (142)
29 1000GENOMES ss1295035077 Aug 21, 2014 (142)
30 DDI ss1426140711 Apr 01, 2015 (144)
31 EVA_GENOME_DK ss1574742381 Apr 01, 2015 (144)
32 EVA_DECODE ss1585645972 Apr 01, 2015 (144)
33 EVA_UK10K_ALSPAC ss1602344847 Apr 01, 2015 (144)
34 EVA_UK10K_TWINSUK ss1645338880 Apr 01, 2015 (144)
35 HAMMER_LAB ss1795862207 Sep 08, 2015 (146)
36 WEILL_CORNELL_DGM ss1919467718 Feb 12, 2016 (147)
37 ILLUMINA ss1958366189 Feb 12, 2016 (147)
38 JJLAB ss2020259098 Sep 14, 2016 (149)
39 USC_VALOUEV ss2148294842 Dec 20, 2016 (150)
40 HUMAN_LONGEVITY ss2170880784 Dec 20, 2016 (150)
41 GRF ss2698294678 Nov 08, 2017 (151)
42 GNOMAD ss2767311955 Nov 08, 2017 (151)
43 AFFY ss2985540505 Nov 08, 2017 (151)
44 SWEGEN ss2988609617 Nov 08, 2017 (151)
45 ILLUMINA ss3021190179 Nov 08, 2017 (151)
46 BIOINF_KMB_FNS_UNIBA ss3023890161 Nov 08, 2017 (151)
47 CSHL ss3343956743 Nov 08, 2017 (151)
48 ILLUMINA ss3626330674 Oct 11, 2018 (152)
49 OMUKHERJEE_ADBS ss3646255202 Oct 11, 2018 (152)
50 ILLUMINA ss3651535833 Oct 11, 2018 (152)
51 EGCUT_WGS ss3656568043 Jul 12, 2019 (153)
52 EVA_DECODE ss3688819280 Jul 12, 2019 (153)
53 ILLUMINA ss3725114486 Jul 12, 2019 (153)
54 ACPOP ss3727946148 Jul 12, 2019 (153)
55 EVA ss3747457691 Jul 12, 2019 (153)
56 PAGE_CC ss3770878842 Jul 12, 2019 (153)
57 KHV_HUMAN_GENOMES ss3800459383 Jul 12, 2019 (153)
58 EVA ss3826693737 Apr 25, 2020 (154)
59 EVA ss3836748608 Apr 25, 2020 (154)
60 EVA ss3842161019 Apr 25, 2020 (154)
61 SGDP_PRJ ss3851098781 Apr 25, 2020 (154)
62 KRGDB ss3896445082 Apr 25, 2020 (154)
63 KOGIC ss3946693316 Apr 25, 2020 (154)
64 FSA-LAB ss3983966668 Apr 25, 2021 (155)
65 FSA-LAB ss3983966669 Apr 25, 2021 (155)
66 EVA ss3984473619 Apr 25, 2021 (155)
67 EVA ss3986015960 Apr 25, 2021 (155)
68 TOPMED ss4486958831 Apr 25, 2021 (155)
69 TOMMO_GENOMICS ss5148875938 Apr 25, 2021 (155)
70 1000G_HIGH_COVERAGE ss5246131881 Oct 12, 2022 (156)
71 EVA ss5325404644 Oct 12, 2022 (156)
72 HUGCELL_USP ss5446534240 Oct 12, 2022 (156)
73 EVA ss5506224019 Oct 12, 2022 (156)
74 1000G_HIGH_COVERAGE ss5520399153 Oct 12, 2022 (156)
75 SANFORD_IMAGENETICS ss5624232555 Oct 12, 2022 (156)
76 SANFORD_IMAGENETICS ss5627637455 Oct 12, 2022 (156)
77 TOMMO_GENOMICS ss5676765081 Oct 12, 2022 (156)
78 YY_MCH ss5801725158 Oct 12, 2022 (156)
79 EVA ss5833398201 Oct 12, 2022 (156)
80 EVA ss5847176314 Oct 12, 2022 (156)
81 EVA ss5847577838 Oct 12, 2022 (156)
82 EVA ss5849328486 Oct 12, 2022 (156)
83 EVA ss5912361218 Oct 12, 2022 (156)
84 EVA ss5939485203 Oct 12, 2022 (156)
85 EVA ss5979308181 Oct 12, 2022 (156)
86 1000Genomes NC_000001.10 - 230850083 Oct 11, 2018 (152)
87 1000Genomes_30x NC_000001.11 - 230714337 Oct 12, 2022 (156)
88 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 230850083 Oct 11, 2018 (152)
89 Genetic variation in the Estonian population NC_000001.10 - 230850083 Oct 11, 2018 (152)
90 The Danish reference pan genome NC_000001.10 - 230850083 Apr 25, 2020 (154)
91 gnomAD - Genomes NC_000001.11 - 230714337 Apr 25, 2021 (155)
92 Genome of the Netherlands Release 5 NC_000001.10 - 230850083 Apr 25, 2020 (154)
93 KOREAN population from KRGDB NC_000001.10 - 230850083 Apr 25, 2020 (154)
94 Korean Genome Project NC_000001.11 - 230714337 Apr 25, 2020 (154)
95 Northern Sweden NC_000001.10 - 230850083 Jul 12, 2019 (153)
96 The PAGE Study NC_000001.11 - 230714337 Jul 12, 2019 (153)
97 CNV burdens in cranial meningiomas NC_000001.10 - 230850083 Apr 25, 2021 (155)
98 PharmGKB Aggregated NC_000001.11 - 230714337 Apr 25, 2020 (154)
99 Qatari NC_000001.10 - 230850083 Apr 25, 2020 (154)
100 SGDP_PRJ NC_000001.10 - 230850083 Apr 25, 2020 (154)
101 Siberian NC_000001.10 - 230850083 Apr 25, 2020 (154)
102 8.3KJPN NC_000001.10 - 230850083 Apr 25, 2021 (155)
103 14KJPN NC_000001.11 - 230714337 Oct 12, 2022 (156)
104 TopMed NC_000001.11 - 230714337 Apr 25, 2021 (155)
105 UK 10K study - Twins NC_000001.10 - 230850083 Oct 11, 2018 (152)
106 A Vietnamese Genetic Variation Database NC_000001.10 - 230850083 Jul 12, 2019 (153)
107 ALFA NC_000001.11 - 230714337 Apr 25, 2021 (155)
108 ClinVar RCV000343947.5 Oct 12, 2022 (156)
109 ClinVar RCV001723880.3 Oct 12, 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)
rs16852410 Oct 07, 2004 (123)
rs36218429 Oct 25, 2006 (127)
rs57840775 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss35217928 NC_000001.8:227156817:C:T NC_000001.11:230714336:C:T (self)
ss109021241, ss111914277, ss119241052, ss165369105, ss199729384, ss276256148, ss1585645972 NC_000001.9:228916705:C:T NC_000001.11:230714336:C:T (self)
5903563, 3264209, 2306291, 1925497, 1426424, 3622476, 1231013, 22941, 1509648, 3115761, 811196, 6845245, 3264209, 710031, ss218933442, ss230940984, ss238547539, ss532918253, ss555199779, ss648772964, ss976246049, ss1068678347, ss1295035077, ss1426140711, ss1574742381, ss1602344847, ss1645338880, ss1795862207, ss1919467718, ss1958366189, ss2020259098, ss2148294842, ss2698294678, ss2767311955, ss2985540505, ss2988609617, ss3021190179, ss3343956743, ss3626330674, ss3646255202, ss3651535833, ss3656568043, ss3727946148, ss3747457691, ss3826693737, ss3836748608, ss3851098781, ss3896445082, ss3983966668, ss3983966669, ss3984473619, ss3986015960, ss5148875938, ss5325404644, ss5506224019, ss5624232555, ss5627637455, ss5833398201, ss5847176314, ss5847577838, ss5939485203, ss5979308181 NC_000001.10:230850082:C:T NC_000001.11:230714336:C:T (self)
RCV000343947.5, RCV001723880.3, 7925088, 42362247, 3071317, 100311, 934, 10602185, 50565166, 9625365534, ss2170880784, ss3023890161, ss3688819280, ss3725114486, ss3770878842, ss3800459383, ss3842161019, ss3946693316, ss4486958831, ss5246131881, ss5446534240, ss5520399153, ss5676765081, ss5801725158, ss5849328486, ss5912361218 NC_000001.11:230714336:C:T NC_000001.11:230714336:C:T (self)
ss6493, ss6695690, ss16338931, ss22886634, ss23235290, ss28460762, ss51853114, ss84151187, ss86211278, ss86215615, ss102649989, ss156402080, ss244302762 NT_167186.1:24367861:C:T NC_000001.11:230714336:C:T (self)
Help

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

10 citations for rs5049
PMID Title Author Year Journal
19770777 Genotype-phenotype analysis of angiotensinogen polymorphisms and essential hypertension: the importance of haplotypes. Watkins WS et al. 2010 Journal of hypertension
21056700 Lack of replication in polymorphisms reported to be associated with atrial fibrillation. Sinner MF et al. 2011 Heart rhythm
21157371 A pharmacogenetic analysis of determinants of hypertension and blood pressure response to angiotensin-converting enzyme inhibitor therapy in patients with vascular disease and healthy individuals. Brugts JJ et al. 2011 Journal of hypertension
21859746 Genetic and BMI risks for predicting blood pressure in three generations of West African Dogon women. Taylor JY et al. 2013 Biological research for nursing
24722536 Relationship of renin-angiotensin-aldosterone system polymorphisms and phenotypes to mortality in Chinese coronary atherosclerosis patients. Jia EZ et al. 2014 Scientific reports
25723521 Polymorphisms of renin-angiotensin-aldosterone system gene in chinese han patients with nonfamilial atrial fibrillation. Zhao LQ et al. 2015 PloS one
26102248 The C4280A (rs5705) gene polymorphism of the renin (REN) gene is associated with risk of developing coronary artery disease, but not with restenosis after coronary stenting. Fragoso JM et al. 2015 Experimental and molecular pathology
26391364 Risk given by AGT polymorphisms in inducing susceptibility to essential hypertension among isolated populations from a remote region of China: A case-control study among the isolated populations. Li Q et al. 2015 Journal of the renin-angiotensin-aldosterone system
26667052 The prevalence of unique SNPs in the renin-angiotensin system highlights the need for pharmacogenetics in Indigenous Australians. Grimson S et al. 2016 Clinical and experimental pharmacology & physiology
29627490 Genetically determined enlargement of carotid body evaluated using computed angiotomography. Jaźwiec P et al. 2018 Respiratory physiology & neurobiology
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