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rs137852583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852583(A;A)
Make rs137852583(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711680
GeneAR
is asnp
is mentioned by
dbSNPrs137852583
ebirs137852583
HLIrs137852583
Exacrs137852583
Varsomers137852583
Maprs137852583
PheGenIrs137852583
hapmaprs137852583
1000 genomesrs137852583
hgdprs137852583
ensemblrs137852583
gopubmedrs137852583
geneviewrs137852583
scholarrs137852583
googlers137852583
pharmgkbrs137852583
gwascentralrs137852583
openSNPrs137852583
23andMers137852583
23andMe allrs137852583
SNP Nexus

SNPshotrs137852583
SNPdbers137852583
MSV3drs137852583
GWAS Ctlgrs137852583
Max Magnitude0
OMIM313700
Desc
Variant0032
Relatedalso
ClinVar
Risk rs137852583(A;A)
Alt rs137852583(A;A)
Reference rs137852583(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.66931522G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010510.3,