Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057523820

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523820(C;T)
Make rs1057523820(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41553740
GeneCASK
is asnp
is mentioned by
dbSNPrs1057523820
dbSNP (old)rs1057523820
ClinGenrs1057523820
ebirs1057523820
HLIrs1057523820
Exacrs1057523820
Gnomadrs1057523820
Varsomers1057523820
Maprs1057523820
PheGenIrs1057523820
Biobankrs1057523820
1000 genomesrs1057523820
hgdprs1057523820
ensemblrs1057523820
gopubmedrs1057523820
geneviewrs1057523820
scholarrs1057523820
googlers1057523820
pharmgkbrs1057523820
gwascentralrs1057523820
openSNPrs1057523820
23andMers1057523820
23andMe allrs1057523820
SNPshotrs1057523820
SNPdbers1057523820
MSV3drs1057523820
GWAS Ctlgrs1057523820
Max Magnitude0
ClinVar
Risk rs1057523820(T;T)
Alt rs1057523820(T;T)
Reference Rs1057523820(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41412993G>A
CLNSRC
CLNACC RCV000443443.1,