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rs794728911

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728911(-;-)
Make rs794728911(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38597888
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728911
ebirs794728911
HLIrs794728911
Exacrs794728911
Varsomers794728911
Maprs794728911
PheGenIrs794728911
hapmaprs794728911
1000 genomesrs794728911
hgdprs794728911
ensemblrs794728911
gopubmedrs794728911
geneviewrs794728911
scholarrs794728911
googlers794728911
pharmgkbrs794728911
gwascentralrs794728911
openSNPrs794728911
23andMers794728911
23andMe allrs794728911
SNP Nexus

SNPshotrs794728911
SNPdbers794728911
MSV3drs794728911
GWAS Ctlgrs794728911
Max Magnitude0
ClinVar
Risk rs794728911(;)
Alt rs794728911(;)
Reference rs794728911(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38639379delC
CLNSRC
CLNACC RCV000183152.2,