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rs118192136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118192136(A;A)
Make rs118192136(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38572184
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192136
ebirs118192136
HLIrs118192136
Exacrs118192136
Varsomers118192136
Maprs118192136
PheGenIrs118192136
hapmaprs118192136
1000 genomesrs118192136
hgdprs118192136
ensemblrs118192136
gopubmedrs118192136
geneviewrs118192136
scholarrs118192136
googlers118192136
pharmgkbrs118192136
gwascentralrs118192136
openSNPrs118192136
23andMers118192136
23andMe allrs118192136
SNP Nexus

SNPshotrs118192136
SNPdbers118192136
MSV3drs118192136
GWAS Ctlgrs118192136
Max Magnitude0
ClinVar
Risk rs118192136(A;A)
Alt rs118192136(A;A)
Reference rs118192136(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.39062824G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056190.1, RCV000119489.1,