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rs118192146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192146(A;G)
Make rs118192146(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38580449
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192146
ebirs118192146
HLIrs118192146
Exacrs118192146
Varsomers118192146
Maprs118192146
PheGenIrs118192146
hapmaprs118192146
1000 genomesrs118192146
hgdprs118192146
ensemblrs118192146
gopubmedrs118192146
geneviewrs118192146
scholarrs118192146
googlers118192146
pharmgkbrs118192146
gwascentralrs118192146
openSNPrs118192146
23andMers118192146
23andMe allrs118192146
SNP Nexus

SNPshotrs118192146
SNPdbers118192146
MSV3drs118192146
GWAS Ctlgrs118192146
Max Magnitude0
ClinVar
Risk rs118192146(G;G)
Alt rs118192146(G;G)
Reference rs118192146(A;A)
Significance Pathogenic
Disease Central core disease not provided
Variation info
Gene RYR1
CLNDBN Central core disease not provided
Reversed 0
HGVS NC_000019.9:g.39071089A>G
CLNSRC UniProtKB (variants)
CLNACC RCV000056251.1, RCV000119535.1,