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rs1057518245

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518245(C;T)
Make rs1057518245(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41531144
GeneCASK
is asnp
is mentioned by
dbSNPrs1057518245
dbSNP (old)rs1057518245
ClinGenrs1057518245
ebirs1057518245
HLIrs1057518245
Exacrs1057518245
Gnomadrs1057518245
Varsomers1057518245
Maprs1057518245
PheGenIrs1057518245
Biobankrs1057518245
1000 genomesrs1057518245
hgdprs1057518245
ensemblrs1057518245
gopubmedrs1057518245
geneviewrs1057518245
scholarrs1057518245
googlers1057518245
pharmgkbrs1057518245
gwascentralrs1057518245
openSNPrs1057518245
23andMers1057518245
23andMe allrs1057518245
SNPshotrs1057518245
SNPdbers1057518245
MSV3drs1057518245
GWAS Ctlgrs1057518245
Max Magnitude0
ClinVar
Risk rs1057518245(T;T)
Alt rs1057518245(T;T)
Reference Rs1057518245(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41390397G>A
CLNSRC
CLNACC RCV000412809.1,