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rs794728837

From SNPedia

Orientationplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs794728837(AG;AG)
Make rs794728837(AG;GC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237783983
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728837
ebirs794728837
HLIrs794728837
Exacrs794728837
Varsomers794728837
Maprs794728837
PheGenIrs794728837
hapmaprs794728837
1000 genomesrs794728837
hgdprs794728837
ensemblrs794728837
gopubmedrs794728837
geneviewrs794728837
scholarrs794728837
googlers794728837
pharmgkbrs794728837
gwascentralrs794728837
openSNPrs794728837
23andMers794728837
23andMe allrs794728837
SNP Nexus

SNPshotrs794728837
SNPdbers794728837
MSV3drs794728837
GWAS Ctlgrs794728837
Max Magnitude0
ClinVar
Risk rs794728837(AG;AG)
Alt rs794728837(AG;AG)
Reference rs794728837(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947283_237947284delGCinsAG
CLNSRC
CLNACC RCV000182900.1,