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rs118192144

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192144(A;G)
Make rs118192144(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38580430
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192144
ebirs118192144
HLIrs118192144
Exacrs118192144
Varsomers118192144
Maprs118192144
PheGenIrs118192144
hapmaprs118192144
1000 genomesrs118192144
hgdprs118192144
ensemblrs118192144
gopubmedrs118192144
geneviewrs118192144
scholarrs118192144
googlers118192144
pharmgkbrs118192144
gwascentralrs118192144
openSNPrs118192144
23andMers118192144
23andMe allrs118192144
SNP Nexus

SNPshotrs118192144
SNPdbers118192144
MSV3drs118192144
GWAS Ctlgrs118192144
Max Magnitude0
ClinVar
Risk rs118192144(G;G)
Alt rs118192144(G;G)
Reference rs118192144(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.39071070A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000056216.1, RCV000119529.1,