Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728747

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728747(G;T)
Make rs794728747(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237639019
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728747
ebirs794728747
HLIrs794728747
Exacrs794728747
Varsomers794728747
Maprs794728747
PheGenIrs794728747
hapmaprs794728747
1000 genomesrs794728747
hgdprs794728747
ensemblrs794728747
gopubmedrs794728747
geneviewrs794728747
scholarrs794728747
googlers794728747
pharmgkbrs794728747
gwascentralrs794728747
openSNPrs794728747
23andMers794728747
23andMe allrs794728747
SNP Nexus

SNPshotrs794728747
SNPdbers794728747
MSV3drs794728747
GWAS Ctlgrs794728747
Max Magnitude0
ClinVar
Risk rs794728747(T;T)
Alt rs794728747(T;T)
Reference rs794728747(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237802319G>T
CLNSRC
CLNACC RCV000182749.2,