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rs794728860

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728860(C;C)
Make rs794728860(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38597943
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728860
ebirs794728860
HLIrs794728860
Exacrs794728860
Varsomers794728860
Maprs794728860
PheGenIrs794728860
hapmaprs794728860
1000 genomesrs794728860
hgdprs794728860
ensemblrs794728860
gopubmedrs794728860
geneviewrs794728860
scholarrs794728860
googlers794728860
pharmgkbrs794728860
gwascentralrs794728860
openSNPrs794728860
23andMers794728860
23andMe allrs794728860
SNP Nexus

SNPshotrs794728860
SNPdbers794728860
MSV3drs794728860
GWAS Ctlgrs794728860
Max Magnitude0
ClinVar
Risk rs794728860(C;C)
Alt rs794728860(C;C)
Reference rs794728860(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene SCN5A
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.38639434C>G
CLNSRC
CLNACC RCV000182995.2,