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

rs137852565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852565(A;A)
Make rs137852565(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67721905
GeneAR
is asnp
is mentioned by
dbSNPrs137852565
ebirs137852565
HLIrs137852565
Exacrs137852565
Varsomers137852565
Maprs137852565
PheGenIrs137852565
hapmaprs137852565
1000 genomesrs137852565
hgdprs137852565
ensemblrs137852565
gopubmedrs137852565
geneviewrs137852565
scholarrs137852565
googlers137852565
pharmgkbrs137852565
gwascentralrs137852565
openSNPrs137852565
23andMers137852565
23andMe allrs137852565
SNP Nexus

SNPshotrs137852565
SNPdbers137852565
MSV3drs137852565
GWAS Ctlgrs137852565
Max Magnitude0
OMIM313700
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137852565(A,C;A,C)
Alt rs137852565(A,C;A,C)
Reference rs137852565(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66941747G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010481.2,