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rs1085307962

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position67711404
GeneAR
is asnp
is mentioned by
dbSNPrs1085307962
dbSNP (old)rs1085307962
ClinGenrs1085307962
ebirs1085307962
HLIrs1085307962
Exacrs1085307962
Gnomadrs1085307962
Varsomers1085307962
Maprs1085307962
PheGenIrs1085307962
Biobankrs1085307962
1000 genomesrs1085307962
hgdprs1085307962
ensemblrs1085307962
gopubmedrs1085307962
geneviewrs1085307962
scholarrs1085307962
googlers1085307962
pharmgkbrs1085307962
gwascentralrs1085307962
openSNPrs1085307962
23andMers1085307962
23andMe allrs1085307962
SNPshotrs1085307962
SNPdbers1085307962
MSV3drs1085307962
GWAS Ctlgrs1085307962
Max Magnitude0
ClinVar
Risk rs1085307962(T;T)
Alt rs1085307962(T;T)
Reference Rs1085307962(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66931246C>T
CLNSRC
CLNACC RCV000489065.1,