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rs587782975

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782975(A;G)
Make rs587782975(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237772024
GeneRYR2
is asnp
is mentioned by
dbSNPrs587782975
ebirs587782975
HLIrs587782975
Exacrs587782975
Varsomers587782975
Maprs587782975
PheGenIrs587782975
hapmaprs587782975
1000 genomesrs587782975
hgdprs587782975
ensemblrs587782975
gopubmedrs587782975
geneviewrs587782975
scholarrs587782975
googlers587782975
pharmgkbrs587782975
gwascentralrs587782975
openSNPrs587782975
23andMers587782975
23andMe allrs587782975
SNP Nexus

SNPshotrs587782975
SNPdbers587782975
MSV3drs587782975
GWAS Ctlgrs587782975
Max Magnitude0
ClinVar
Risk rs587782975(G;G)
Alt rs587782975(G;G)
Reference rs587782975(A;A)
Significance Probable-Pathogenic
Disease Ventricular tachycardia not specified
Variation info
Gene RYR2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 1 not specified
Reversed 0
HGVS NC_000001.10:g.237935324A>G
CLNSRC
CLNACC RCV000143948.1, RCV000182797.2,