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rs587784376

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784376(C;T)
Make rs587784376(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38475382
GeneRYR1
is asnp
is mentioned by
dbSNPrs587784376
ebirs587784376
HLIrs587784376
Exacrs587784376
Varsomers587784376
Maprs587784376
PheGenIrs587784376
hapmaprs587784376
1000 genomesrs587784376
hgdprs587784376
ensemblrs587784376
gopubmedrs587784376
geneviewrs587784376
scholarrs587784376
googlers587784376
pharmgkbrs587784376
gwascentralrs587784376
openSNPrs587784376
23andMers587784376
23andMe allrs587784376
SNP Nexus

SNPshotrs587784376
SNPdbers587784376
MSV3drs587784376
GWAS Ctlgrs587784376
Max Magnitude0
ClinVar
Risk rs587784376(T;T)
Alt rs587784376(T;T)
Reference rs587784376(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38966022C>T
CLNSRC
CLNACC RCV000147427.1,