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rs1064794065

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position67717601
GeneAR
is asnp
is mentioned by
dbSNPrs1064794065
dbSNP (old)rs1064794065
ClinGenrs1064794065
ebirs1064794065
HLIrs1064794065
Exacrs1064794065
Gnomadrs1064794065
Varsomers1064794065
Maprs1064794065
PheGenIrs1064794065
Biobankrs1064794065
1000 genomesrs1064794065
hgdprs1064794065
ensemblrs1064794065
gopubmedrs1064794065
geneviewrs1064794065
scholarrs1064794065
googlers1064794065
pharmgkbrs1064794065
gwascentralrs1064794065
openSNPrs1064794065
23andMers1064794065
23andMe allrs1064794065
SNPshotrs1064794065
SNPdbers1064794065
MSV3drs1064794065
GWAS Ctlgrs1064794065
Max Magnitude0
ClinVar
Risk rs1064794065(A;A)
Alt rs1064794065(A;A)
Reference Rs1064794065(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66937443C>A
CLNSRC
CLNACC RCV000481893.1,