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rs186906598

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs186906598(A;A)
Make rs186906598(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237627977
GeneRYR2
is asnp
is mentioned by
dbSNPrs186906598
ebirs186906598
HLIrs186906598
Exacrs186906598
Varsomers186906598
Maprs186906598
PheGenIrs186906598
hapmaprs186906598
1000 genomesrs186906598
hgdprs186906598
ensemblrs186906598
gopubmedrs186906598
geneviewrs186906598
scholarrs186906598
googlers186906598
pharmgkbrs186906598
gwascentralrs186906598
openSNPrs186906598
23andMers186906598
23andMe allrs186906598
SNP Nexus

SNPshotrs186906598
SNPdbers186906598
MSV3drs186906598
GWAS Ctlgrs186906598
Max Magnitude0
ClinVar
Risk rs186906598(A;A)
Alt rs186906598(A;A)
Reference rs186906598(G;G)
Significance Probable-non-pathogenic
Disease not specified Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN not specified Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237791277G>A
CLNSRC
CLNACC RCV000036777.3, RCV000171764.2,