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rs137852595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852595(C;T)
Make rs137852595(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711653
GeneAR
is asnp
is mentioned by
dbSNPrs137852595
ebirs137852595
HLIrs137852595
Exacrs137852595
Varsomers137852595
Maprs137852595
PheGenIrs137852595
hapmaprs137852595
1000 genomesrs137852595
hgdprs137852595
ensemblrs137852595
gopubmedrs137852595
geneviewrs137852595
scholarrs137852595
googlers137852595
pharmgkbrs137852595
gwascentralrs137852595
openSNPrs137852595
23andMers137852595
23andMe allrs137852595
SNP Nexus

SNPshotrs137852595
SNPdbers137852595
MSV3drs137852595
GWAS Ctlgrs137852595
Max Magnitude0
OMIM313700
Desc
Variant0050
Relatedalso
ClinVar
Risk rs137852595(T;T)
Alt rs137852595(T;T)
Reference rs137852595(C;C)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66931495C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010526.4,