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rs587784379

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784379(C;G)
Make rs587784379(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38516111
GeneRYR1
is asnp
is mentioned by
dbSNPrs587784379
ebirs587784379
HLIrs587784379
Exacrs587784379
Varsomers587784379
Maprs587784379
PheGenIrs587784379
hapmaprs587784379
1000 genomesrs587784379
hgdprs587784379
ensemblrs587784379
gopubmedrs587784379
geneviewrs587784379
scholarrs587784379
googlers587784379
pharmgkbrs587784379
gwascentralrs587784379
openSNPrs587784379
23andMers587784379
23andMe allrs587784379
SNP Nexus

SNPshotrs587784379
SNPdbers587784379
MSV3drs587784379
GWAS Ctlgrs587784379
Max Magnitude0
ClinVar
Risk rs587784379(G;G)
Alt rs587784379(G;G)
Reference rs587784379(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.39006751C>G
CLNSRC
CLNACC RCV000147451.1,