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rs794728880

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728880(A;A)
Make rs794728880(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38560145
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728880
ebirs794728880
HLIrs794728880
Exacrs794728880
Varsomers794728880
Maprs794728880
PheGenIrs794728880
hapmaprs794728880
1000 genomesrs794728880
hgdprs794728880
ensemblrs794728880
gopubmedrs794728880
geneviewrs794728880
scholarrs794728880
googlers794728880
pharmgkbrs794728880
gwascentralrs794728880
openSNPrs794728880
23andMers794728880
23andMe allrs794728880
SNP Nexus

SNPshotrs794728880
SNPdbers794728880
MSV3drs794728880
GWAS Ctlgrs794728880
Max Magnitude0
ClinVar
Risk rs794728880(A;A)
Alt rs794728880(A;A)
Reference rs794728880(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38601636A>T
CLNSRC
CLNACC RCV000183067.1,