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rs137852584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852584(A;A)
Make rs137852584(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711459
GeneAR
is asnp
is mentioned by
dbSNPrs137852584
ebirs137852584
HLIrs137852584
Exacrs137852584
Varsomers137852584
Maprs137852584
PheGenIrs137852584
hapmaprs137852584
1000 genomesrs137852584
hgdprs137852584
ensemblrs137852584
gopubmedrs137852584
geneviewrs137852584
scholarrs137852584
googlers137852584
pharmgkbrs137852584
gwascentralrs137852584
openSNPrs137852584
23andMers137852584
23andMe allrs137852584
SNP Nexus

SNPshotrs137852584
SNPdbers137852584
MSV3drs137852584
GWAS Ctlgrs137852584
Max Magnitude0
OMIM313700
Desc
Variant0033
Relatedalso
ClinVar
Risk rs137852584(A;A)
Alt rs137852584(A;A)
Reference rs137852584(G;G)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene AR
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000023.10:g.66931301G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010483.4,