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rs121917813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121917813(A;T)
Make rs121917813(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position116172437
GeneAGTR2
is asnp
is mentioned by
dbSNPrs121917813
ebirs121917813
HLIrs121917813
Exacrs121917813
Varsomers121917813
Maprs121917813
PheGenIrs121917813
hapmaprs121917813
1000 genomesrs121917813
hgdprs121917813
ensemblrs121917813
gopubmedrs121917813
geneviewrs121917813
scholarrs121917813
googlers121917813
pharmgkbrs121917813
gwascentralrs121917813
openSNPrs121917813
23andMers121917813
23andMe allrs121917813
SNP Nexus

SNPshotrs121917813
SNPdbers121917813
MSV3drs121917813
GWAS Ctlgrs121917813
Max Magnitude0
ClinVar
Risk rs121917813(T;T)
Alt rs121917813(T;T)
Reference rs121917813(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene AGTR2
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.115303690A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000088654.2,