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rs794728868

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728868(C;C)
Make rs794728868(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585722
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728868
ebirs794728868
HLIrs794728868
Exacrs794728868
Varsomers794728868
Maprs794728868
PheGenIrs794728868
hapmaprs794728868
1000 genomesrs794728868
hgdprs794728868
ensemblrs794728868
gopubmedrs794728868
geneviewrs794728868
scholarrs794728868
googlers794728868
pharmgkbrs794728868
gwascentralrs794728868
openSNPrs794728868
23andMers794728868
23andMe allrs794728868
SNP Nexus

SNPshotrs794728868
SNPdbers794728868
MSV3drs794728868
GWAS Ctlgrs794728868
Max Magnitude0
ClinVar
Risk rs794728868(C;C)
Alt rs794728868(C;C)
Reference rs794728868(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38627213A>G
CLNSRC
CLNACC RCV000183011.1,