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rs1064795250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position67723818
GeneAR
is asnp
is mentioned by
dbSNPrs1064795250
dbSNP (old)rs1064795250
ClinGenrs1064795250
ebirs1064795250
HLIrs1064795250
Exacrs1064795250
Gnomadrs1064795250
Varsomers1064795250
LitVarrs1064795250
Maprs1064795250
PheGenIrs1064795250
Biobankrs1064795250
1000 genomesrs1064795250
hgdprs1064795250
ensemblrs1064795250
gopubmedrs1064795250
geneviewrs1064795250
scholarrs1064795250
googlers1064795250
pharmgkbrs1064795250
gwascentralrs1064795250
openSNPrs1064795250
23andMers1064795250
23andMe allrs1064795250
SNPshotrs1064795250
SNPdbers1064795250
MSV3drs1064795250
GWAS Ctlgrs1064795250
Max Magnitude0
ClinVar
Risk rs1064795250(A;A)
Alt rs1064795250(A;A)
Reference Rs1064795250(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66943660C>A
CLNSRC
CLNACC RCV000481757.1,