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rs1064796884

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position41531102
GeneCASK
is asnp
is mentioned by
dbSNPrs1064796884
dbSNP (old)rs1064796884
ClinGenrs1064796884
ebirs1064796884
HLIrs1064796884
Exacrs1064796884
Gnomadrs1064796884
Varsomers1064796884
Maprs1064796884
PheGenIrs1064796884
Biobankrs1064796884
1000 genomesrs1064796884
hgdprs1064796884
ensemblrs1064796884
gopubmedrs1064796884
geneviewrs1064796884
scholarrs1064796884
googlers1064796884
pharmgkbrs1064796884
gwascentralrs1064796884
openSNPrs1064796884
23andMers1064796884
23andMe allrs1064796884
SNPshotrs1064796884
SNPdbers1064796884
MSV3drs1064796884
GWAS Ctlgrs1064796884
Max Magnitude0
ClinVar
Risk rs1064796884(A;A)
Alt rs1064796884(A;A)
Reference Rs1064796884(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41390355C>T
CLNSRC
CLNACC RCV000481292.1,