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rs794728940

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728940(C;T)
Make rs794728940(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550542
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728940
ebirs794728940
HLIrs794728940
Exacrs794728940
Varsomers794728940
Maprs794728940
PheGenIrs794728940
hapmaprs794728940
1000 genomesrs794728940
hgdprs794728940
ensemblrs794728940
gopubmedrs794728940
geneviewrs794728940
scholarrs794728940
googlers794728940
pharmgkbrs794728940
gwascentralrs794728940
openSNPrs794728940
23andMers794728940
23andMe allrs794728940
SNP Nexus

SNPshotrs794728940
SNPdbers794728940
MSV3drs794728940
GWAS Ctlgrs794728940
Max Magnitude0
ClinVar
Risk rs794728940(T;T)
Alt rs794728940(T;T)
Reference rs794728940(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592033G>A
CLNSRC
CLNACC RCV000183202.1,