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rs794728834

From SNPedia

Orientationplus
Geno Mag Summary
(GTC;GTC) 0 common in clinvar
Make rs794728834(-;-)
Make rs794728834(-;CGT)
Make rs794728834(CGT;CGT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237639043
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728834
ebirs794728834
HLIrs794728834
Exacrs794728834
Varsomers794728834
Maprs794728834
PheGenIrs794728834
hapmaprs794728834
1000 genomesrs794728834
hgdprs794728834
ensemblrs794728834
gopubmedrs794728834
geneviewrs794728834
scholarrs794728834
googlers794728834
pharmgkbrs794728834
gwascentralrs794728834
openSNPrs794728834
23andMers794728834
23andMe allrs794728834
SNP Nexus

SNPshotrs794728834
SNPdbers794728834
MSV3drs794728834
GWAS Ctlgrs794728834
Max Magnitude0
ClinVar
Risk rs794728834(;)
Alt rs794728834(;)
Reference rs794728834(GTC;GTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237802343_237802345delCGT
CLNSRC
CLNACC RCV000182897.1,