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rs1064794937

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position41660507
GeneCASK
is asnp
is mentioned by
dbSNPrs1064794937
dbSNP (old)rs1064794937
ClinGenrs1064794937
ebirs1064794937
HLIrs1064794937
Exacrs1064794937
Gnomadrs1064794937
Varsomers1064794937
Maprs1064794937
PheGenIrs1064794937
Biobankrs1064794937
1000 genomesrs1064794937
hgdprs1064794937
ensemblrs1064794937
gopubmedrs1064794937
geneviewrs1064794937
scholarrs1064794937
googlers1064794937
pharmgkbrs1064794937
gwascentralrs1064794937
openSNPrs1064794937
23andMers1064794937
23andMe allrs1064794937
SNPshotrs1064794937
SNPdbers1064794937
MSV3drs1064794937
GWAS Ctlgrs1064794937
Max Magnitude0
ClinVar
Risk rs1064794937(T;T)
Alt rs1064794937(T;T)
Reference Rs1064794937(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41519760G>A
CLNSRC
CLNACC RCV000485733.1,