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rs137852582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852582(A;G)
Make rs137852582(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723786
GeneAR
is asnp
is mentioned by
dbSNPrs137852582
ebirs137852582
HLIrs137852582
Exacrs137852582
Varsomers137852582
Maprs137852582
PheGenIrs137852582
hapmaprs137852582
1000 genomesrs137852582
hgdprs137852582
ensemblrs137852582
gopubmedrs137852582
geneviewrs137852582
scholarrs137852582
googlers137852582
pharmgkbrs137852582
gwascentralrs137852582
openSNPrs137852582
23andMers137852582
23andMe allrs137852582
SNP Nexus

SNPshotrs137852582
SNPdbers137852582
MSV3drs137852582
GWAS Ctlgrs137852582
Max Magnitude0
OMIM313700
Desc
Variant0031
Relatedalso
ClinVar
Risk rs137852582(G;G)
Alt rs137852582(G;G)
Reference Rs137852582(A;A)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene AR
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000023.10:g.66943628A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010509.2,