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rs193922820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922820(C;C)
Make rs193922820(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38502527
GeneRYR1
is asnp
is mentioned by
dbSNPrs193922820
ebirs193922820
HLIrs193922820
Exacrs193922820
Varsomers193922820
Maprs193922820
PheGenIrs193922820
hapmaprs193922820
1000 genomesrs193922820
hgdprs193922820
ensemblrs193922820
gopubmedrs193922820
geneviewrs193922820
scholarrs193922820
googlers193922820
pharmgkbrs193922820
gwascentralrs193922820
openSNPrs193922820
23andMers193922820
23andMe allrs193922820
SNP Nexus

SNPshotrs193922820
SNPdbers193922820
MSV3drs193922820
GWAS Ctlgrs193922820
Max Magnitude0
ClinVar
Risk rs193922820(C;C)
Alt rs193922820(C;C)
Reference rs193922820(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.38993167G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000056180.1, RCV000119724.1,