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rs1064793293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position48689434
GeneWAS
is asnp
is mentioned by
dbSNPrs1064793293
dbSNP (old)rs1064793293
ClinGenrs1064793293
ebirs1064793293
HLIrs1064793293
Exacrs1064793293
Gnomadrs1064793293
Varsomers1064793293
LitVarrs1064793293
Maprs1064793293
PheGenIrs1064793293
Biobankrs1064793293
1000 genomesrs1064793293
hgdprs1064793293
ensemblrs1064793293
gopubmedrs1064793293
geneviewrs1064793293
scholarrs1064793293
googlers1064793293
pharmgkbrs1064793293
gwascentralrs1064793293
openSNPrs1064793293
23andMers1064793293
23andMe allrs1064793293
SNPshotrs1064793293
SNPdbers1064793293
MSV3drs1064793293
GWAS Ctlgrs1064793293
Max Magnitude0
ClinVar
Risk rs1064793293(A;A)
Alt rs1064793293(A;A)
Reference Rs1064793293(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WAS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48547823G>A
CLNSRC
CLNACC RCV000482823.1,