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

rs794728915

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728915(A;CCC)
Make rs794728915(CCC;CCC)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38581047
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728915
ebirs794728915
HLIrs794728915
Exacrs794728915
Varsomers794728915
Maprs794728915
PheGenIrs794728915
hapmaprs794728915
1000 genomesrs794728915
hgdprs794728915
ensemblrs794728915
gopubmedrs794728915
geneviewrs794728915
scholarrs794728915
googlers794728915
pharmgkbrs794728915
gwascentralrs794728915
openSNPrs794728915
23andMers794728915
23andMe allrs794728915
SNP Nexus

SNPshotrs794728915
SNPdbers794728915
MSV3drs794728915
GWAS Ctlgrs794728915
Max Magnitude0
ClinVar
Risk rs794728915(CCC;CCC)
Alt rs794728915(CCC;CCC)
Reference rs794728915(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38622538delTinsGGG
CLNSRC
CLNACC RCV000183156.1,