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rs121917810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917810(G;T)
Make rs121917810(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position116172342
GeneAGTR2
is asnp
is mentioned by
dbSNPrs121917810
ebirs121917810
HLIrs121917810
Exacrs121917810
Varsomers121917810
Maprs121917810
PheGenIrs121917810
hapmaprs121917810
1000 genomesrs121917810
hgdprs121917810
ensemblrs121917810
gopubmedrs121917810
geneviewrs121917810
scholarrs121917810
googlers121917810
pharmgkbrs121917810
gwascentralrs121917810
openSNPrs121917810
23andMers121917810
23andMe allrs121917810
SNP Nexus

SNPshotrs121917810
SNPdbers121917810
MSV3drs121917810
GWAS Ctlgrs121917810
Max Magnitude0
ClinVar
Risk rs121917810(T;T)
Alt rs121917810(T;T)
Reference rs121917810(G;G)
Significance Non-pathogenic
Disease not provided not specified
Variation info
Gene AGTR2
CLNDBN not provided not specified
Reversed 0
HGVS NC_000023.10:g.115303595G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000088651.2, RCV000116283.1,