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rs606231226

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231226(C;T)
Make rs606231226(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position154305155
GeneDPP6
is asnp
is mentioned by
dbSNPrs606231226
ebirs606231226
HLIrs606231226
Exacrs606231226
Varsomers606231226
Maprs606231226
PheGenIrs606231226
hapmaprs606231226
1000 genomesrs606231226
hgdprs606231226
ensemblrs606231226
gopubmedrs606231226
geneviewrs606231226
scholarrs606231226
googlers606231226
pharmgkbrs606231226
gwascentralrs606231226
openSNPrs606231226
23andMers606231226
23andMe allrs606231226
SNP Nexus

SNPshotrs606231226
SNPdbers606231226
MSV3drs606231226
GWAS Ctlgrs606231226
Max Magnitude0
ClinVar
Risk rs606231226(T;T)
Alt rs606231226(T;T)
Reference rs606231226(C;C)
Significance Pathogenic
Disease Ventricular fibrillation
Variation info
Gene DPP6
CLNDBN Ventricular fibrillation, paroxysmal familial, 2
Reversed 0
HGVS NC_000007.14:g.154305155C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018285.28,