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rs1057517923

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517923(A;A)
Make rs1057517923(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41569668
GeneCASK
is asnp
is mentioned by
dbSNPrs1057517923
dbSNP (old)rs1057517923
ClinGenrs1057517923
ebirs1057517923
HLIrs1057517923
Exacrs1057517923
Gnomadrs1057517923
Varsomers1057517923
LitVarrs1057517923
Maprs1057517923
PheGenIrs1057517923
Biobankrs1057517923
1000 genomesrs1057517923
hgdprs1057517923
ensemblrs1057517923
gopubmedrs1057517923
geneviewrs1057517923
scholarrs1057517923
googlers1057517923
pharmgkbrs1057517923
gwascentralrs1057517923
openSNPrs1057517923
23andMers1057517923
23andMe allrs1057517923
SNPshotrs1057517923
SNPdbers1057517923
MSV3drs1057517923
GWAS Ctlgrs1057517923
Max Magnitude0
ClinVar
Risk rs1057517923(A;A)
Alt rs1057517923(A;A)
Reference Rs1057517923(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41428921C>T
CLNSRC
CLNACC RCV000414089.1,