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rs794728873

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728873(C;T)
Make rs794728873(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38575410
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728873
ebirs794728873
HLIrs794728873
Exacrs794728873
Varsomers794728873
Maprs794728873
PheGenIrs794728873
hapmaprs794728873
1000 genomesrs794728873
hgdprs794728873
ensemblrs794728873
gopubmedrs794728873
geneviewrs794728873
scholarrs794728873
googlers794728873
pharmgkbrs794728873
gwascentralrs794728873
openSNPrs794728873
23andMers794728873
23andMe allrs794728873
SNP Nexus

SNPshotrs794728873
SNPdbers794728873
MSV3drs794728873
GWAS Ctlgrs794728873
Max Magnitude0
ClinVar
Risk rs794728873(T;T)
Alt rs794728873(T;T)
Reference rs794728873(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38616901G>A
CLNSRC
CLNACC RCV000183024.1,