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rs1064794901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position21984384
GeneSMS
is asnp
is mentioned by
dbSNPrs1064794901
dbSNP (old)rs1064794901
ClinGenrs1064794901
ebirs1064794901
HLIrs1064794901
Exacrs1064794901
Gnomadrs1064794901
Varsomers1064794901
Maprs1064794901
PheGenIrs1064794901
Biobankrs1064794901
1000 genomesrs1064794901
hgdprs1064794901
ensemblrs1064794901
gopubmedrs1064794901
geneviewrs1064794901
scholarrs1064794901
googlers1064794901
pharmgkbrs1064794901
gwascentralrs1064794901
openSNPrs1064794901
23andMers1064794901
23andMe allrs1064794901
SNPshotrs1064794901
SNPdbers1064794901
MSV3drs1064794901
GWAS Ctlgrs1064794901
Max Magnitude0
ClinVar
Risk rs1064794901(T;T)
Alt rs1064794901(T;T)
Reference Rs1064794901(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22002502G>T
CLNSRC
CLNACC RCV000480904.1,