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rs794728721

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728721(A;A)
Make rs794728721(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237445489
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728721
ebirs794728721
HLIrs794728721
Exacrs794728721
Varsomers794728721
Maprs794728721
PheGenIrs794728721
hapmaprs794728721
1000 genomesrs794728721
hgdprs794728721
ensemblrs794728721
gopubmedrs794728721
geneviewrs794728721
scholarrs794728721
googlers794728721
pharmgkbrs794728721
gwascentralrs794728721
openSNPrs794728721
23andMers794728721
23andMe allrs794728721
SNP Nexus

SNPshotrs794728721
SNPdbers794728721
MSV3drs794728721
GWAS Ctlgrs794728721
Max Magnitude0
ClinVar
Risk rs794728721(A;A)
Alt rs794728721(A;A)
Reference rs794728721(G;G)
Significance Other
Disease not provided Long QT syndrome
Variation info
Gene RYR2
CLNDBN not provided Long QT syndrome
Reversed 0
HGVS NC_000001.10:g.237608789G>A
CLNSRC
CLNACC RCV000182681.1, RCV000190228.1,