Have questions? Visit https://www.reddit.com/r/SNPedia

rs118192126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192126(A;G)
Make rs118192126(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38519295
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192126
ebirs118192126
HLIrs118192126
Exacrs118192126
Varsomers118192126
Maprs118192126
PheGenIrs118192126
hapmaprs118192126
1000 genomesrs118192126
hgdprs118192126
ensemblrs118192126
gopubmedrs118192126
geneviewrs118192126
scholarrs118192126
googlers118192126
pharmgkbrs118192126
gwascentralrs118192126
openSNPrs118192126
23andMers118192126
23andMe allrs118192126
SNP Nexus

SNPshotrs118192126
SNPdbers118192126
MSV3drs118192126
GWAS Ctlgrs118192126
Max Magnitude0
ClinVar
Risk rs118192126(G;G)
Alt rs118192126(G;G)
Reference rs118192126(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.39009935A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000056203.1, RCV000119402.1,