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rs1085307685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position67717552
GeneAR
is asnp
is mentioned by
dbSNPrs1085307685
dbSNP (classic)rs1085307685
ClinGenrs1085307685
ebirs1085307685
HLIrs1085307685
Exacrs1085307685
Gnomadrs1085307685
Varsomers1085307685
LitVarrs1085307685
Maprs1085307685
PheGenIrs1085307685
Biobankrs1085307685
1000 genomesrs1085307685
hgdprs1085307685
ensemblrs1085307685
geneviewrs1085307685
scholarrs1085307685
googlers1085307685
pharmgkbrs1085307685
gwascentralrs1085307685
openSNPrs1085307685
23andMers1085307685
SNPshotrs1085307685
SNPdbers1085307685
MSV3drs1085307685
GWAS Ctlgrs1085307685
Max Magnitude0
ClinVar
Risk rs1085307685(G;G)
Alt rs1085307685(G;G)
Reference Rs1085307685(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66937394A>G
CLNSRC
CLNACC RCV000488944.1,