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rs118192113

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118192113(A;A)
Make rs118192113(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position38442395
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192113
ebirs118192113
HLIrs118192113
Exacrs118192113
Varsomers118192113
Maprs118192113
PheGenIrs118192113
hapmaprs118192113
1000 genomesrs118192113
hgdprs118192113
ensemblrs118192113
gopubmedrs118192113
geneviewrs118192113
scholarrs118192113
googlers118192113
pharmgkbrs118192113
gwascentralrs118192113
openSNPrs118192113
23andMers118192113
23andMe allrs118192113
SNP Nexus

SNPshotrs118192113
SNPdbers118192113
MSV3drs118192113
GWAS Ctlgrs118192113
Max Magnitude0
ClinVar
Risk rs118192113(A;A)
Alt rs118192113(A;A)
Reference rs118192113(C;C)
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.38933035C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056240.1, RCV000119591.1,