Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852576(A;A)
Make rs137852576(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67686067
GeneAR
is asnp
is mentioned by
dbSNPrs137852576
ebirs137852576
HLIrs137852576
Exacrs137852576
Varsomers137852576
Maprs137852576
PheGenIrs137852576
hapmaprs137852576
1000 genomesrs137852576
hgdprs137852576
ensemblrs137852576
gopubmedrs137852576
geneviewrs137852576
scholarrs137852576
googlers137852576
pharmgkbrs137852576
gwascentralrs137852576
openSNPrs137852576
23andMers137852576
23andMe allrs137852576
SNP Nexus

SNPshotrs137852576
SNPdbers137852576
MSV3drs137852576
GWAS Ctlgrs137852576
Max Magnitude0
OMIM313700
Desc
Variant0024
Relatedalso
ClinVar
Risk rs137852576(A;A)
Alt rs137852576(A;A)
Reference rs137852576(G;G)
Significance Pathogenic
Disease Androgen insensitivity
Variation info
Gene AR
CLNDBN Androgen insensitivity, partial, with breast cancer
Reversed 0
HGVS NC_000023.10:g.66905909G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010502.2,