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rs118192120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118192120(A;A)
Make rs118192120(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38483311
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192120
ebirs118192120
HLIrs118192120
Exacrs118192120
Varsomers118192120
Maprs118192120
PheGenIrs118192120
hapmaprs118192120
1000 genomesrs118192120
hgdprs118192120
ensemblrs118192120
gopubmedrs118192120
geneviewrs118192120
scholarrs118192120
googlers118192120
pharmgkbrs118192120
gwascentralrs118192120
openSNPrs118192120
23andMers118192120
23andMe allrs118192120
SNP Nexus

SNPshotrs118192120
SNPdbers118192120
MSV3drs118192120
GWAS Ctlgrs118192120
Max Magnitude0
ClinVar
Risk rs118192120(A;A)
Alt rs118192120(A;A)
Reference rs118192120(G;G)
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.38973951G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056170.1, RCV000119622.1,