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rs193922884

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922884(C;T)
Make rs193922884(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38580503
GeneRYR1
is asnp
is mentioned by
dbSNPrs193922884
ebirs193922884
HLIrs193922884
Exacrs193922884
Varsomers193922884
Maprs193922884
PheGenIrs193922884
hapmaprs193922884
1000 genomesrs193922884
hgdprs193922884
ensemblrs193922884
gopubmedrs193922884
geneviewrs193922884
scholarrs193922884
googlers193922884
pharmgkbrs193922884
gwascentralrs193922884
openSNPrs193922884
23andMers193922884
23andMe allrs193922884
SNP Nexus

SNPshotrs193922884
SNPdbers193922884
MSV3drs193922884
GWAS Ctlgrs193922884
Max Magnitude0
ClinVar
Risk rs193922884(T;T)
Alt rs193922884(T;T)
Reference rs193922884(C;C)
Significance Probable-Pathogenic
Disease not provided Central core disease
Variation info
Gene RYR1
CLNDBN not provided Central core disease
Reversed 0
HGVS NC_000019.9:g.39071143C>T
CLNSRC
CLNACC RCV000119538.1, RCV000233721.1,