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rs794728942

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728942(-;-)
Make rs794728942(-;AC)
Make rs794728942(AC;AC)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585772
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728942
ebirs794728942
HLIrs794728942
Exacrs794728942
Varsomers794728942
Maprs794728942
PheGenIrs794728942
hapmaprs794728942
1000 genomesrs794728942
hgdprs794728942
ensemblrs794728942
gopubmedrs794728942
geneviewrs794728942
scholarrs794728942
googlers794728942
pharmgkbrs794728942
gwascentralrs794728942
openSNPrs794728942
23andMers794728942
23andMe allrs794728942
SNP Nexus

SNPshotrs794728942
SNPdbers794728942
MSV3drs794728942
GWAS Ctlgrs794728942
Max Magnitude0
ClinVar
Risk rs794728942(AC;AC)
Alt rs794728942(AC;AC)
Reference rs794728942(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38627264_38627265dupGT
CLNSRC
CLNACC RCV000183204.1,