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rs137852599

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852599(A;C)
Make rs137852599(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711585
GeneAR
is asnp
is mentioned by
dbSNPrs137852599
ebirs137852599
HLIrs137852599
Exacrs137852599
Varsomers137852599
Maprs137852599
PheGenIrs137852599
hapmaprs137852599
1000 genomesrs137852599
hgdprs137852599
ensemblrs137852599
gopubmedrs137852599
geneviewrs137852599
scholarrs137852599
googlers137852599
pharmgkbrs137852599
gwascentralrs137852599
openSNPrs137852599
23andMers137852599
23andMe allrs137852599
SNP Nexus

SNPshotrs137852599
SNPdbers137852599
MSV3drs137852599
GWAS Ctlgrs137852599
Max Magnitude0
OMIM313700
Desc
Variant0055
Relatedalso
ClinVar
Risk rs137852599(C;C)
Alt rs137852599(C;C)
Reference rs137852599(A;A)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66931427A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010530.3,