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rs1057524485

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524485(A;C)
Make rs1057524485(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41569748
GeneCASK
is asnp
is mentioned by
dbSNPrs1057524485
dbSNP (old)rs1057524485
ClinGenrs1057524485
ebirs1057524485
HLIrs1057524485
Exacrs1057524485
Gnomadrs1057524485
Varsomers1057524485
Maprs1057524485
PheGenIrs1057524485
Biobankrs1057524485
1000 genomesrs1057524485
hgdprs1057524485
ensemblrs1057524485
gopubmedrs1057524485
geneviewrs1057524485
scholarrs1057524485
googlers1057524485
pharmgkbrs1057524485
gwascentralrs1057524485
openSNPrs1057524485
23andMers1057524485
23andMe allrs1057524485
SNPshotrs1057524485
SNPdbers1057524485
MSV3drs1057524485
GWAS Ctlgrs1057524485
Max Magnitude0
ClinVar
Risk rs1057524485(C;C)
Alt rs1057524485(C;C)
Reference Rs1057524485(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41429001T>G
CLNSRC
CLNACC RCV000419173.1,