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rs1064796879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position41578363
GeneCASK
is asnp
is mentioned by
dbSNPrs1064796879
dbSNP (old)rs1064796879
ClinGenrs1064796879
ebirs1064796879
HLIrs1064796879
Exacrs1064796879
Gnomadrs1064796879
Varsomers1064796879
Maprs1064796879
PheGenIrs1064796879
Biobankrs1064796879
1000 genomesrs1064796879
hgdprs1064796879
ensemblrs1064796879
gopubmedrs1064796879
geneviewrs1064796879
scholarrs1064796879
googlers1064796879
pharmgkbrs1064796879
gwascentralrs1064796879
openSNPrs1064796879
23andMers1064796879
23andMe allrs1064796879
SNPshotrs1064796879
SNPdbers1064796879
MSV3drs1064796879
GWAS Ctlgrs1064796879
Max Magnitude0
ClinVar
Risk rs1064796879(T;T)
Alt rs1064796879(T;T)
Reference Rs1064796879(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41437616G>A
CLNSRC
CLNACC RCV000485707.1,