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rs587784375

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587784375(-;-)
Make rs587784375(-;G)
Make rs587784375(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38473705
GeneRYR1
is asnp
is mentioned by
dbSNPrs587784375
ebirs587784375
HLIrs587784375
Exacrs587784375
Varsomers587784375
Maprs587784375
PheGenIrs587784375
hapmaprs587784375
1000 genomesrs587784375
hgdprs587784375
ensemblrs587784375
gopubmedrs587784375
geneviewrs587784375
scholarrs587784375
googlers587784375
pharmgkbrs587784375
gwascentralrs587784375
openSNPrs587784375
23andMers587784375
23andMe allrs587784375
SNP Nexus

SNPshotrs587784375
SNPdbers587784375
MSV3drs587784375
GWAS Ctlgrs587784375
Max Magnitude0
ClinVar
Risk rs587784375(G;G)
Alt rs587784375(G;G)
Reference rs587784375(;)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38964345dupG
CLNSRC
CLNACC RCV000147426.1,