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

rs146876145

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146876145(C;T)
Make rs146876145(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position38586140
GeneRYR1
is asnp
is mentioned by
dbSNPrs146876145
ebirs146876145
HLIrs146876145
Exacrs146876145
Varsomers146876145
Maprs146876145
PheGenIrs146876145
hapmaprs146876145
1000 genomesrs146876145
hgdprs146876145
ensemblrs146876145
gopubmedrs146876145
geneviewrs146876145
scholarrs146876145
googlers146876145
pharmgkbrs146876145
gwascentralrs146876145
openSNPrs146876145
23andMers146876145
23andMe allrs146876145
SNP Nexus

SNPshotrs146876145
SNPdbers146876145
MSV3drs146876145
GWAS Ctlgrs146876145
Max Magnitude0
ClinVar
Risk rs146876145(T;T)
Alt rs146876145(T;T)
Reference rs146876145(C;C)
Significance Probable-Pathogenic
Disease not provided Malignant hyperthermia Central core disease
Variation info
Gene RYR1
CLNDBN not provided Malignant hyperthermia, susceptibility to, 1 Central core disease
Reversed 0
HGVS NC_000019.9:g.39076780C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000119571.1, RCV000148804.2, RCV000173939.1,