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

rs118192155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118192155(A;A)
Make rs118192155(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position38585055
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192155
ebirs118192155
HLIrs118192155
Exacrs118192155
Varsomers118192155
Maprs118192155
PheGenIrs118192155
hapmaprs118192155
1000 genomesrs118192155
hgdprs118192155
ensemblrs118192155
gopubmedrs118192155
geneviewrs118192155
scholarrs118192155
googlers118192155
pharmgkbrs118192155
gwascentralrs118192155
openSNPrs118192155
23andMers118192155
23andMe allrs118192155
SNP Nexus

SNPshotrs118192155
SNPdbers118192155
MSV3drs118192155
GWAS Ctlgrs118192155
Max Magnitude0
ClinVar
Risk rs118192155(A;A)
Alt rs118192155(A;A)
Reference rs118192155(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.39075695C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056244.1, RCV000119558.1,