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rs267606698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606698(A;A)
Make rs267606698(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201066917
GeneCACNA1S
is asnp
is mentioned by
dbSNPrs267606698
ebirs267606698
HLIrs267606698
Exacrs267606698
Varsomers267606698
Maprs267606698
PheGenIrs267606698
hapmaprs267606698
1000 genomesrs267606698
hgdprs267606698
ensemblrs267606698
gopubmedrs267606698
geneviewrs267606698
scholarrs267606698
googlers267606698
pharmgkbrs267606698
gwascentralrs267606698
openSNPrs267606698
23andMers267606698
23andMe allrs267606698
SNP Nexus

SNPshotrs267606698
SNPdbers267606698
MSV3drs267606698
GWAS Ctlgrs267606698
Max Magnitude0
ClinVar
Risk rs267606698(A;A)
Alt rs267606698(A;A)
Reference rs267606698(T;T)
Significance Pathogenic
Disease Hypokalemic periodic paralysis 1
Variation info
Gene CACNA1S
CLNDBN Hypokalemic periodic paralysis 1
Reversed 1
HGVS NC_000001.10:g.201036045A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019198.29,