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rs137852579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852579(C;C)
Make rs137852579(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711549
GeneAR
is asnp
is mentioned by
dbSNPrs137852579
ebirs137852579
HLIrs137852579
Exacrs137852579
Varsomers137852579
Maprs137852579
PheGenIrs137852579
hapmaprs137852579
1000 genomesrs137852579
hgdprs137852579
ensemblrs137852579
gopubmedrs137852579
geneviewrs137852579
scholarrs137852579
googlers137852579
pharmgkbrs137852579
gwascentralrs137852579
openSNPrs137852579
23andMers137852579
23andMe allrs137852579
SNP Nexus

SNPshotrs137852579
SNPdbers137852579
MSV3drs137852579
GWAS Ctlgrs137852579
Max Magnitude0
OMIM313700
Desc
Variant0028
Relatedalso
ClinVar
Risk rs137852579(C;C)
Alt rs137852579(C;C)
Reference rs137852579(T;T)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66931391T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010506.2,