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rs137852580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852580(C;G)
Make rs137852580(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723711
GeneAR
is asnp
is mentioned by
dbSNPrs137852580
ebirs137852580
HLIrs137852580
Exacrs137852580
Varsomers137852580
Maprs137852580
PheGenIrs137852580
hapmaprs137852580
1000 genomesrs137852580
hgdprs137852580
ensemblrs137852580
gopubmedrs137852580
geneviewrs137852580
scholarrs137852580
googlers137852580
pharmgkbrs137852580
gwascentralrs137852580
openSNPrs137852580
23andMers137852580
23andMe allrs137852580
SNP Nexus

SNPshotrs137852580
SNPdbers137852580
MSV3drs137852580
GWAS Ctlgrs137852580
Max Magnitude0
OMIM313700
Desc
Variant0029
Relatedalso
ClinVar
Risk rs137852580(G;G)
Alt rs137852580(G;G)
Reference rs137852580(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.66943553C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010507.2,