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rs370634440

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370634440(A;A)
Make rs370634440(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38463499
GeneRYR1
is asnp
is mentioned by
dbSNPrs370634440
ebirs370634440
HLIrs370634440
Exacrs370634440
Varsomers370634440
Maprs370634440
PheGenIrs370634440
hapmaprs370634440
1000 genomesrs370634440
hgdprs370634440
ensemblrs370634440
gopubmedrs370634440
geneviewrs370634440
scholarrs370634440
googlers370634440
pharmgkbrs370634440
gwascentralrs370634440
openSNPrs370634440
23andMers370634440
23andMe allrs370634440
SNP Nexus

SNPshotrs370634440
SNPdbers370634440
MSV3drs370634440
GWAS Ctlgrs370634440
Max Magnitude0
ClinVar
Risk rs370634440(A,T;A,T)
Alt rs370634440(A,T;A,T)
Reference rs370634440(G;G)
Significance Probable-Pathogenic
Disease Myopathy
Variation info
Gene RYR1
CLNDBN Myopathy
Reversed 0
HGVS NC_000019.9:g.38954139G>A
CLNSRC
CLNACC RCV000195228.1,