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rs368874586

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368874586(A;A)
Make rs368874586(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38586150
GeneRYR1
is asnp
is mentioned by
dbSNPrs368874586
ebirs368874586
HLIrs368874586
Exacrs368874586
Varsomers368874586
Maprs368874586
PheGenIrs368874586
hapmaprs368874586
1000 genomesrs368874586
hgdprs368874586
ensemblrs368874586
gopubmedrs368874586
geneviewrs368874586
scholarrs368874586
googlers368874586
pharmgkbrs368874586
gwascentralrs368874586
openSNPrs368874586
23andMers368874586
23andMe allrs368874586
SNP Nexus

SNPshotrs368874586
SNPdbers368874586
MSV3drs368874586
GWAS Ctlgrs368874586
Max Magnitude0
ClinVar
Risk rs368874586(A,G;A,G)
Alt rs368874586(A,G;A,G)
Reference rs368874586(C;C)
Significance Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene RYR1
CLNDBN not provided Inborn genetic diseases
Reversed 0
HGVS NC_000019.9:g.39076790C>G
CLNSRC
CLNACC RCV000182613.1, RCV000210545.1,