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rs118192159

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118192159(C;G)
Make rs118192159(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38585948
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192159
ebirs118192159
HLIrs118192159
Exacrs118192159
Varsomers118192159
Maprs118192159
PheGenIrs118192159
hapmaprs118192159
1000 genomesrs118192159
hgdprs118192159
ensemblrs118192159
gopubmedrs118192159
geneviewrs118192159
scholarrs118192159
googlers118192159
pharmgkbrs118192159
gwascentralrs118192159
openSNPrs118192159
23andMers118192159
23andMe allrs118192159
SNP Nexus

SNPshotrs118192159
SNPdbers118192159
MSV3drs118192159
GWAS Ctlgrs118192159
Max Magnitude0
ClinVar
Risk rs118192159(G,T;G,T)
Alt rs118192159(G,T;G,T)
Reference rs118192159(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.39076588C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000056202.1, RCV000119564.1,