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rs797045935

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045935(A;A)
Make rs797045935(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38506860
GeneRYR1
is asnp
is mentioned by
dbSNPrs797045935
ebirs797045935
HLIrs797045935
Exacrs797045935
Varsomers797045935
Maprs797045935
PheGenIrs797045935
hapmaprs797045935
1000 genomesrs797045935
hgdprs797045935
ensemblrs797045935
gopubmedrs797045935
geneviewrs797045935
scholarrs797045935
googlers797045935
pharmgkbrs797045935
gwascentralrs797045935
openSNPrs797045935
23andMers797045935
23andMe allrs797045935
SNP Nexus

SNPshotrs797045935
SNPdbers797045935
MSV3drs797045935
GWAS Ctlgrs797045935
Max Magnitude0
ClinVar
Risk rs797045935(A;A)
Alt rs797045935(A;A)
Reference rs797045935(C;C)
Significance Pathogenic
Disease Myopathy
Variation info
Gene RYR1
CLNDBN Myopathy
Reversed 0
HGVS NC_000019.9:g.38997500C>A
CLNSRC
CLNACC RCV000194443.1,