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rs794728910

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728910(-;-)
Make rs794728910(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38603849
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728910
ebirs794728910
HLIrs794728910
Exacrs794728910
Varsomers794728910
Maprs794728910
PheGenIrs794728910
hapmaprs794728910
1000 genomesrs794728910
hgdprs794728910
ensemblrs794728910
gopubmedrs794728910
geneviewrs794728910
scholarrs794728910
googlers794728910
pharmgkbrs794728910
gwascentralrs794728910
openSNPrs794728910
23andMers794728910
23andMe allrs794728910
SNP Nexus

SNPshotrs794728910
SNPdbers794728910
MSV3drs794728910
GWAS Ctlgrs794728910
Max Magnitude0
ClinVar
Risk rs794728910(;)
Alt rs794728910(;)
Reference rs794728910(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38645340delG
CLNSRC
CLNACC RCV000183150.2,