Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064795456

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position7325371
GeneSTS
is asnp
is mentioned by
dbSNPrs1064795456
dbSNP (old)rs1064795456
ClinGenrs1064795456
ebirs1064795456
HLIrs1064795456
Exacrs1064795456
Gnomadrs1064795456
Varsomers1064795456
Maprs1064795456
PheGenIrs1064795456
Biobankrs1064795456
1000 genomesrs1064795456
hgdprs1064795456
ensemblrs1064795456
gopubmedrs1064795456
geneviewrs1064795456
scholarrs1064795456
googlers1064795456
pharmgkbrs1064795456
gwascentralrs1064795456
openSNPrs1064795456
23andMers1064795456
23andMe allrs1064795456
SNPshotrs1064795456
SNPdbers1064795456
MSV3drs1064795456
GWAS Ctlgrs1064795456
Max Magnitude0
ClinVar
Risk rs1064795456(T;T)
Alt rs1064795456(T;T)
Reference Rs1064795456(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.7243412C>T
CLNSRC
CLNACC RCV000481064.1,