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rs794728785

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728785(C;T)
Make rs794728785(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784013
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728785
ebirs794728785
HLIrs794728785
Exacrs794728785
Varsomers794728785
Maprs794728785
PheGenIrs794728785
hapmaprs794728785
1000 genomesrs794728785
hgdprs794728785
ensemblrs794728785
gopubmedrs794728785
geneviewrs794728785
scholarrs794728785
googlers794728785
pharmgkbrs794728785
gwascentralrs794728785
openSNPrs794728785
23andMers794728785
23andMe allrs794728785
SNP Nexus

SNPshotrs794728785
SNPdbers794728785
MSV3drs794728785
GWAS Ctlgrs794728785
Max Magnitude0
ClinVar
Risk rs794728785(T;T)
Alt rs794728785(T;T)
Reference rs794728785(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947313C>T
CLNSRC
CLNACC RCV000182815.1,