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rs1064793480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position67721934
GeneAR
is asnp
is mentioned by
dbSNPrs1064793480
dbSNP (old)rs1064793480
ClinGenrs1064793480
ebirs1064793480
HLIrs1064793480
Exacrs1064793480
Gnomadrs1064793480
Varsomers1064793480
Maprs1064793480
PheGenIrs1064793480
Biobankrs1064793480
1000 genomesrs1064793480
hgdprs1064793480
ensemblrs1064793480
gopubmedrs1064793480
geneviewrs1064793480
scholarrs1064793480
googlers1064793480
pharmgkbrs1064793480
gwascentralrs1064793480
openSNPrs1064793480
23andMers1064793480
23andMe allrs1064793480
SNPshotrs1064793480
SNPdbers1064793480
MSV3drs1064793480
GWAS Ctlgrs1064793480
Max Magnitude0
ClinVar
Risk rs1064793480(A;A)
Alt rs1064793480(A;A)
Reference Rs1064793480(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66941776G>A
CLNSRC
CLNACC RCV000482241.1,