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rs121917811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121917811(A;G)
Make rs121917811(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position116173289
GeneAGTR2
is asnp
is mentioned by
dbSNPrs121917811
ebirs121917811
HLIrs121917811
Exacrs121917811
Varsomers121917811
Maprs121917811
PheGenIrs121917811
hapmaprs121917811
1000 genomesrs121917811
hgdprs121917811
ensemblrs121917811
gopubmedrs121917811
geneviewrs121917811
scholarrs121917811
googlers121917811
pharmgkbrs121917811
gwascentralrs121917811
openSNPrs121917811
23andMers121917811
23andMe allrs121917811
SNP Nexus

SNPshotrs121917811
SNPdbers121917811
MSV3drs121917811
GWAS Ctlgrs121917811
Max Magnitude0
ClinVar
Risk rs121917811(G;G)
Alt rs121917811(G;G)
Reference rs121917811(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene AGTR2
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.115304542A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000088655.2,