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rs797045934

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045934(A;A)
Make rs797045934(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38467813
GeneRYR1
is asnp
is mentioned by
dbSNPrs797045934
ebirs797045934
HLIrs797045934
Exacrs797045934
Varsomers797045934
Maprs797045934
PheGenIrs797045934
hapmaprs797045934
1000 genomesrs797045934
hgdprs797045934
ensemblrs797045934
gopubmedrs797045934
geneviewrs797045934
scholarrs797045934
googlers797045934
pharmgkbrs797045934
gwascentralrs797045934
openSNPrs797045934
23andMers797045934
23andMe allrs797045934
SNP Nexus

SNPshotrs797045934
SNPdbers797045934
MSV3drs797045934
GWAS Ctlgrs797045934
Max Magnitude0
ClinVar
Risk rs797045934(A;A)
Alt rs797045934(A;A)
Reference rs797045934(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene RYR1
CLNDBN Myopathy
Reversed 0
HGVS NC_000019.9:g.38958453G>A
CLNSRC
CLNACC RCV000194934.1,