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rs398122845

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122845(A;T)
Make rs398122845(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position41524036
GeneCASK
is asnp
is mentioned by
dbSNPrs398122845
ebirs398122845
HLIrs398122845
Exacrs398122845
Varsomers398122845
Maprs398122845
PheGenIrs398122845
hapmaprs398122845
1000 genomesrs398122845
hgdprs398122845
ensemblrs398122845
gopubmedrs398122845
geneviewrs398122845
scholarrs398122845
googlers398122845
pharmgkbrs398122845
gwascentralrs398122845
openSNPrs398122845
23andMers398122845
23andMe allrs398122845
SNP Nexus

SNPshotrs398122845
SNPdbers398122845
MSV3drs398122845
GWAS Ctlgrs398122845
Max Magnitude0
ClinVar
Risk rs398122845(T;T)
Alt rs398122845(T;T)
Reference rs398122845(A;A)
Significance Pathogenic
Disease FG syndrome 4 not specified
Variation info
Gene CASK
CLNDBN FG syndrome 4 not specified
Reversed 1
HGVS NC_000023.10:g.41383289T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022830.22, RCV000145403.1,