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rs759736132

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs759736132(C;C)
Make rs759736132(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41531041
GeneCASK
is asnp
is mentioned by
dbSNPrs759736132
ebirs759736132
HLIrs759736132
Exacrs759736132
Varsomers759736132
Maprs759736132
PheGenIrs759736132
hapmaprs759736132
1000 genomesrs759736132
hgdprs759736132
ensemblrs759736132
gopubmedrs759736132
geneviewrs759736132
scholarrs759736132
googlers759736132
pharmgkbrs759736132
gwascentralrs759736132
openSNPrs759736132
23andMers759736132
23andMe allrs759736132
SNP Nexus

SNPshotrs759736132
SNPdbers759736132
MSV3drs759736132
GWAS Ctlgrs759736132
Max Magnitude0
ClinVar
Risk rs759736132(C;C)
Alt rs759736132(C;C)
Reference rs759736132(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CASK
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.41390294T>C
CLNSRC
CLNACC RCV000190700.1,