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rs794728750

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728750(A;A)
Make rs794728750(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237639036
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728750
ebirs794728750
HLIrs794728750
Exacrs794728750
Varsomers794728750
Maprs794728750
PheGenIrs794728750
hapmaprs794728750
1000 genomesrs794728750
hgdprs794728750
ensemblrs794728750
gopubmedrs794728750
geneviewrs794728750
scholarrs794728750
googlers794728750
pharmgkbrs794728750
gwascentralrs794728750
openSNPrs794728750
23andMers794728750
23andMe allrs794728750
SNP Nexus

SNPshotrs794728750
SNPdbers794728750
MSV3drs794728750
GWAS Ctlgrs794728750
Max Magnitude0
ClinVar
Risk rs794728750(A;A)
Alt rs794728750(A;A)
Reference rs794728750(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237802336C>A
CLNSRC
CLNACC RCV000182752.2,