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rs794728885

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728885(A;T)
Make rs794728885(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38556454
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728885
ebirs794728885
HLIrs794728885
Exacrs794728885
Varsomers794728885
Maprs794728885
PheGenIrs794728885
hapmaprs794728885
1000 genomesrs794728885
hgdprs794728885
ensemblrs794728885
gopubmedrs794728885
geneviewrs794728885
scholarrs794728885
googlers794728885
pharmgkbrs794728885
gwascentralrs794728885
openSNPrs794728885
23andMers794728885
23andMe allrs794728885
SNP Nexus

SNPshotrs794728885
SNPdbers794728885
MSV3drs794728885
GWAS Ctlgrs794728885
Max Magnitude0
ClinVar
Risk rs794728885(T;T)
Alt rs794728885(T;T)
Reference rs794728885(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38597945T>A
CLNSRC
CLNACC RCV000183076.2,