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rs786205455

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205455(C;T)
Make rs786205455(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237709002
GeneRYR2
is asnp
is mentioned by
dbSNPrs786205455
ebirs786205455
HLIrs786205455
Exacrs786205455
Varsomers786205455
Maprs786205455
PheGenIrs786205455
hapmaprs786205455
1000 genomesrs786205455
hgdprs786205455
ensemblrs786205455
gopubmedrs786205455
geneviewrs786205455
scholarrs786205455
googlers786205455
pharmgkbrs786205455
gwascentralrs786205455
openSNPrs786205455
23andMers786205455
23andMe allrs786205455
SNP Nexus

SNPshotrs786205455
SNPdbers786205455
MSV3drs786205455
GWAS Ctlgrs786205455
Max Magnitude0
ClinVar
Risk rs786205455(T;T)
Alt rs786205455(T;T)
Reference rs786205455(C;C)
Significance Probable-Pathogenic
Disease not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene RYR2
CLNDBN not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.237872302C>T
CLNSRC
CLNACC RCV000171173.1, RCV000208443.1,