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

rs118192132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs118192132(A;A)
Make rs118192132(A;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position38572163
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192132
ebirs118192132
HLIrs118192132
Exacrs118192132
Varsomers118192132
Maprs118192132
PheGenIrs118192132
hapmaprs118192132
1000 genomesrs118192132
hgdprs118192132
ensemblrs118192132
gopubmedrs118192132
geneviewrs118192132
scholarrs118192132
googlers118192132
pharmgkbrs118192132
gwascentralrs118192132
openSNPrs118192132
23andMers118192132
23andMe allrs118192132
SNP Nexus

SNPshotrs118192132
SNPdbers118192132
MSV3drs118192132
GWAS Ctlgrs118192132
Max Magnitude0
ClinVar
Risk rs118192132(A;A)
Alt rs118192132(A;A)
Reference rs118192132(T;T)
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.39062803T>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056249.1, RCV000119485.1,