Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728875

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728875(C;C)
Make rs794728875(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38575334
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728875
ebirs794728875
HLIrs794728875
Exacrs794728875
Varsomers794728875
Maprs794728875
PheGenIrs794728875
hapmaprs794728875
1000 genomesrs794728875
hgdprs794728875
ensemblrs794728875
gopubmedrs794728875
geneviewrs794728875
scholarrs794728875
googlers794728875
pharmgkbrs794728875
gwascentralrs794728875
openSNPrs794728875
23andMers794728875
23andMe allrs794728875
SNP Nexus

SNPshotrs794728875
SNPdbers794728875
MSV3drs794728875
GWAS Ctlgrs794728875
Max Magnitude0
ClinVar
Risk rs794728875(C;C)
Alt rs794728875(C;C)
Reference rs794728875(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38616825A>G
CLNSRC
CLNACC RCV000183040.2,