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

rs137852577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852577(C;T)
Make rs137852577(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67722898
GeneAR
is asnp
is mentioned by
dbSNPrs137852577
ebirs137852577
HLIrs137852577
Exacrs137852577
Varsomers137852577
Maprs137852577
PheGenIrs137852577
hapmaprs137852577
1000 genomesrs137852577
hgdprs137852577
ensemblrs137852577
gopubmedrs137852577
geneviewrs137852577
scholarrs137852577
googlers137852577
pharmgkbrs137852577
gwascentralrs137852577
openSNPrs137852577
23andMers137852577
23andMe allrs137852577
SNP Nexus

SNPshotrs137852577
SNPdbers137852577
MSV3drs137852577
GWAS Ctlgrs137852577
Max Magnitude0
OMIM313700
Desc
Variant0026
Relatedalso
ClinVar
Risk rs137852577(T;T)
Alt rs137852577(T;T)
Reference rs137852577(C;C)
Significance Pathogenic
Disease Reifenstein syndrome Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66942740C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010504.2, RCV000010529.2,