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

rs137852562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852562(C;T)
Make rs137852562(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67721837
GeneAR
is asnp
is mentioned by
dbSNPrs137852562
ebirs137852562
HLIrs137852562
Exacrs137852562
Varsomers137852562
Maprs137852562
PheGenIrs137852562
hapmaprs137852562
1000 genomesrs137852562
hgdprs137852562
ensemblrs137852562
gopubmedrs137852562
geneviewrs137852562
scholarrs137852562
googlers137852562
pharmgkbrs137852562
gwascentralrs137852562
openSNPrs137852562
23andMers137852562
23andMe allrs137852562
SNP Nexus

SNPshotrs137852562
SNPdbers137852562
MSV3drs137852562
GWAS Ctlgrs137852562
Max Magnitude0
OMIM313700
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852562(T;T)
Alt rs137852562(T;T)
Reference rs137852562(C;C)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66941679C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010478.3,