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

rs137852568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852568(A;T)
Make rs137852568(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723728
GeneAR
is asnp
is mentioned by
dbSNPrs137852568
ebirs137852568
HLIrs137852568
Exacrs137852568
Varsomers137852568
Maprs137852568
PheGenIrs137852568
hapmaprs137852568
1000 genomesrs137852568
hgdprs137852568
ensemblrs137852568
gopubmedrs137852568
geneviewrs137852568
scholarrs137852568
googlers137852568
pharmgkbrs137852568
gwascentralrs137852568
openSNPrs137852568
23andMers137852568
23andMe allrs137852568
SNP Nexus

SNPshotrs137852568
SNPdbers137852568
MSV3drs137852568
GWAS Ctlgrs137852568
Max Magnitude0
OMIM313700
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137852568(T;T)
Alt rs137852568(T;T)
Reference rs137852568(A;A)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66943570A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010485.2,