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rs137852578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852578(A;G)
Make rs137852578(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723710
GeneAR
is asnp
is mentioned by
dbSNPrs137852578
ebirs137852578
HLIrs137852578
Exacrs137852578
Varsomers137852578
Maprs137852578
PheGenIrs137852578
hapmaprs137852578
1000 genomesrs137852578
hgdprs137852578
ensemblrs137852578
gopubmedrs137852578
geneviewrs137852578
scholarrs137852578
googlers137852578
pharmgkbrs137852578
gwascentralrs137852578
openSNPrs137852578
23andMers137852578
23andMe allrs137852578
SNP Nexus

SNPshotrs137852578
SNPdbers137852578
MSV3drs137852578
GWAS Ctlgrs137852578
Max Magnitude0
OMIM313700
Desc
Variant0027
Relatedalso
ClinVar
Risk rs137852578(G;G)
Alt rs137852578(G;G)
Reference rs137852578(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.66943552A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010505.4,