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rs794728843

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728843(A;A)
Make rs794728843(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38620842
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728843
ebirs794728843
HLIrs794728843
Exacrs794728843
Varsomers794728843
Maprs794728843
PheGenIrs794728843
hapmaprs794728843
1000 genomesrs794728843
hgdprs794728843
ensemblrs794728843
gopubmedrs794728843
geneviewrs794728843
scholarrs794728843
googlers794728843
pharmgkbrs794728843
gwascentralrs794728843
openSNPrs794728843
23andMers794728843
23andMe allrs794728843
SNP Nexus

SNPshotrs794728843
SNPdbers794728843
MSV3drs794728843
GWAS Ctlgrs794728843
Max Magnitude0
ClinVar
Risk rs794728843(A;A)
Alt rs794728843(A;A)
Reference rs794728843(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38662333C>T
CLNSRC
CLNACC RCV000182920.2,