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rs587784373

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784373(A;A)
Make rs587784373(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38580458
GeneRYR1
is asnp
is mentioned by
dbSNPrs587784373
ebirs587784373
HLIrs587784373
Exacrs587784373
Varsomers587784373
Maprs587784373
PheGenIrs587784373
hapmaprs587784373
1000 genomesrs587784373
hgdprs587784373
ensemblrs587784373
gopubmedrs587784373
geneviewrs587784373
scholarrs587784373
googlers587784373
pharmgkbrs587784373
gwascentralrs587784373
openSNPrs587784373
23andMers587784373
23andMe allrs587784373
SNP Nexus

SNPshotrs587784373
SNPdbers587784373
MSV3drs587784373
GWAS Ctlgrs587784373
Max Magnitude0
ClinVar
Risk rs587784373(A;A)
Alt rs587784373(A;A)
Reference rs587784373(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.39071098G>A
CLNSRC
CLNACC RCV000147415.1,