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rs794728783

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728783(C;T)
Make rs794728783(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237783984
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728783
ebirs794728783
HLIrs794728783
Exacrs794728783
Varsomers794728783
Maprs794728783
PheGenIrs794728783
hapmaprs794728783
1000 genomesrs794728783
hgdprs794728783
ensemblrs794728783
gopubmedrs794728783
geneviewrs794728783
scholarrs794728783
googlers794728783
pharmgkbrs794728783
gwascentralrs794728783
openSNPrs794728783
23andMers794728783
23andMe allrs794728783
SNP Nexus

SNPshotrs794728783
SNPdbers794728783
MSV3drs794728783
GWAS Ctlgrs794728783
Max Magnitude0
ClinVar
Risk rs794728783(T;T)
Alt rs794728783(T;T)
Reference rs794728783(C;C)
Significance Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene RYR2
CLNDBN not provided Long QT syndrome
Reversed 0
HGVS NC_000001.10:g.237947284C>T
CLNSRC
CLNACC RCV000182811.1, RCV000190127.1,