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rs794728817

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728817(C;T)
Make rs794728817(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237469125
GeneMIR4428, RYR2
is asnp
is mentioned by
dbSNPrs794728817
ebirs794728817
HLIrs794728817
Exacrs794728817
Varsomers794728817
Maprs794728817
PheGenIrs794728817
hapmaprs794728817
1000 genomesrs794728817
hgdprs794728817
ensemblrs794728817
gopubmedrs794728817
geneviewrs794728817
scholarrs794728817
googlers794728817
pharmgkbrs794728817
gwascentralrs794728817
openSNPrs794728817
23andMers794728817
23andMe allrs794728817
SNP Nexus

SNPshotrs794728817
SNPdbers794728817
MSV3drs794728817
GWAS Ctlgrs794728817
Max Magnitude0
ClinVar
Risk rs794728817(T;T)
Alt rs794728817(T;T)
Reference rs794728817(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2 MIR4428
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237632425C>T
CLNSRC
CLNACC RCV000182864.1,