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rs794728863

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728863(A;A)
Make rs794728863(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38587506
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728863
ebirs794728863
HLIrs794728863
Exacrs794728863
Varsomers794728863
Maprs794728863
PheGenIrs794728863
hapmaprs794728863
1000 genomesrs794728863
hgdprs794728863
ensemblrs794728863
gopubmedrs794728863
geneviewrs794728863
scholarrs794728863
googlers794728863
pharmgkbrs794728863
gwascentralrs794728863
openSNPrs794728863
23andMers794728863
23andMe allrs794728863
SNP Nexus

SNPshotrs794728863
SNPdbers794728863
MSV3drs794728863
GWAS Ctlgrs794728863
Max Magnitude0
ClinVar
Risk rs794728863(A;A)
Alt rs794728863(A;A)
Reference rs794728863(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38628997A>T
CLNSRC
CLNACC RCV000183001.2,