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rs35474657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35474657(C;T)
Make rs35474657(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position116173251
GeneAGTR2
is asnp
is mentioned by
dbSNPrs35474657
ebirs35474657
HLIrs35474657
Exacrs35474657
Varsomers35474657
Maprs35474657
PheGenIrs35474657
hapmaprs35474657
1000 genomesrs35474657
hgdprs35474657
ensemblrs35474657
gopubmedrs35474657
geneviewrs35474657
scholarrs35474657
googlers35474657
pharmgkbrs35474657
gwascentralrs35474657
openSNPrs35474657
23andMers35474657
23andMe allrs35474657
SNP Nexus

SNPshotrs35474657
SNPdbers35474657
MSV3drs35474657
GWAS Ctlgrs35474657
GMAF0.002418
Max Magnitude0
OMIM300034
Desc
Variant0003
Relatedalso


ClinVar
Risk rs35474657(T;T)
Alt rs35474657(T;T)
Reference rs35474657(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AGTR2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.115304504G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000088653.2,