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rs137852581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852581(C;T)
Make rs137852581(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723701
GeneAR
is asnp
is mentioned by
dbSNPrs137852581
ebirs137852581
HLIrs137852581
Exacrs137852581
Varsomers137852581
Maprs137852581
PheGenIrs137852581
hapmaprs137852581
1000 genomesrs137852581
hgdprs137852581
ensemblrs137852581
gopubmedrs137852581
geneviewrs137852581
scholarrs137852581
googlers137852581
pharmgkbrs137852581
gwascentralrs137852581
openSNPrs137852581
23andMers137852581
23andMe allrs137852581
SNP Nexus

SNPshotrs137852581
SNPdbers137852581
MSV3drs137852581
GWAS Ctlgrs137852581
Max Magnitude0
OMIM313700
Desc
Variant0030
Relatedalso
ClinVar
Risk rs137852581(T;T)
Alt rs137852581(T;T)
Reference rs137852581(C;C)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene AR
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000023.10:g.66943543C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010508.4,