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

rs794728941

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728941(C;G)
Make rs794728941(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550387
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728941
ebirs794728941
HLIrs794728941
Exacrs794728941
Varsomers794728941
Maprs794728941
PheGenIrs794728941
hapmaprs794728941
1000 genomesrs794728941
hgdprs794728941
ensemblrs794728941
gopubmedrs794728941
geneviewrs794728941
scholarrs794728941
googlers794728941
pharmgkbrs794728941
gwascentralrs794728941
openSNPrs794728941
23andMers794728941
23andMe allrs794728941
SNP Nexus

SNPshotrs794728941
SNPdbers794728941
MSV3drs794728941
GWAS Ctlgrs794728941
Max Magnitude0
ClinVar
Risk rs794728941(G;G)
Alt rs794728941(G;G)
Reference rs794728941(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene SCN5A
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.38591878G>C
CLNSRC
CLNACC RCV000183203.2,