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rs587784374

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587784374(-;-)
Make rs587784374(-;C)
Make rs587784374(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38473412
GeneRYR1
is asnp
is mentioned by
dbSNPrs587784374
ebirs587784374
HLIrs587784374
Exacrs587784374
Varsomers587784374
Maprs587784374
PheGenIrs587784374
hapmaprs587784374
1000 genomesrs587784374
hgdprs587784374
ensemblrs587784374
gopubmedrs587784374
geneviewrs587784374
scholarrs587784374
googlers587784374
pharmgkbrs587784374
gwascentralrs587784374
openSNPrs587784374
23andMers587784374
23andMe allrs587784374
SNP Nexus

SNPshotrs587784374
SNPdbers587784374
MSV3drs587784374
GWAS Ctlgrs587784374
Max Magnitude0
ClinVar
Risk rs587784374(C;C)
Alt rs587784374(C;C)
Reference rs587784374(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38964052dupC
CLNSRC
CLNACC RCV000147422.1,