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

rs794728931

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728931(A;A)
Make rs794728931(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38575388
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728931
ebirs794728931
HLIrs794728931
Exacrs794728931
Varsomers794728931
Maprs794728931
PheGenIrs794728931
hapmaprs794728931
1000 genomesrs794728931
hgdprs794728931
ensemblrs794728931
gopubmedrs794728931
geneviewrs794728931
scholarrs794728931
googlers794728931
pharmgkbrs794728931
gwascentralrs794728931
openSNPrs794728931
23andMers794728931
23andMe allrs794728931
SNP Nexus

SNPshotrs794728931
SNPdbers794728931
MSV3drs794728931
GWAS Ctlgrs794728931
Max Magnitude0
ClinVar
Risk rs794728931(A;A)
Alt rs794728931(A;A)
Reference rs794728931(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38616879C>T
CLNSRC
CLNACC RCV000183182.1,