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rs794728883

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728883(C;C)
Make rs794728883(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38556475
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728883
ebirs794728883
HLIrs794728883
Exacrs794728883
Varsomers794728883
Maprs794728883
PheGenIrs794728883
hapmaprs794728883
1000 genomesrs794728883
hgdprs794728883
ensemblrs794728883
gopubmedrs794728883
geneviewrs794728883
scholarrs794728883
googlers794728883
pharmgkbrs794728883
gwascentralrs794728883
openSNPrs794728883
23andMers794728883
23andMe allrs794728883
SNP Nexus

SNPshotrs794728883
SNPdbers794728883
MSV3drs794728883
GWAS Ctlgrs794728883
Max Magnitude0
ClinVar
Risk rs794728883(C;C)
Alt rs794728883(C;C)
Reference rs794728883(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38597966A>G
CLNSRC
CLNACC RCV000183074.1,