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rs1057521754

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521754(C;C)
Make rs1057521754(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41671467
GeneCASK
is asnp
is mentioned by
dbSNPrs1057521754
dbSNP (old)rs1057521754
ClinGenrs1057521754
ebirs1057521754
HLIrs1057521754
Exacrs1057521754
Gnomadrs1057521754
Varsomers1057521754
LitVarrs1057521754
Maprs1057521754
PheGenIrs1057521754
Biobankrs1057521754
1000 genomesrs1057521754
hgdprs1057521754
ensemblrs1057521754
gopubmedrs1057521754
geneviewrs1057521754
scholarrs1057521754
googlers1057521754
pharmgkbrs1057521754
gwascentralrs1057521754
openSNPrs1057521754
23andMers1057521754
23andMe allrs1057521754
SNPshotrs1057521754
SNPdbers1057521754
MSV3drs1057521754
GWAS Ctlgrs1057521754
Max Magnitude0
ClinVar
Risk rs1057521754(C;C)
Alt rs1057521754(C;C)
Reference Rs1057521754(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.41530720C>G
CLNSRC
CLNACC RCV000427392.1,