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rs794728928

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728928(A;A)
Make rs794728928(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38598916
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728928
ebirs794728928
HLIrs794728928
Exacrs794728928
Varsomers794728928
Maprs794728928
PheGenIrs794728928
hapmaprs794728928
1000 genomesrs794728928
hgdprs794728928
ensemblrs794728928
gopubmedrs794728928
geneviewrs794728928
scholarrs794728928
googlers794728928
pharmgkbrs794728928
gwascentralrs794728928
openSNPrs794728928
23andMers794728928
23andMe allrs794728928
SNP Nexus

SNPshotrs794728928
SNPdbers794728928
MSV3drs794728928
GWAS Ctlgrs794728928
Max Magnitude0
ClinVar
Risk rs794728928(A;A)
Alt rs794728928(A;A)
Reference rs794728928(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38640407A>T
CLNSRC
CLNACC RCV000183176.1,