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rs794728921

From SNPedia

Orientationminus
Geno Mag Summary
(AGG;AGG) 0 common in clinvar
Make rs794728921(-;-)
Make rs794728921(-;AGG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38560428
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728921
ebirs794728921
HLIrs794728921
Exacrs794728921
Varsomers794728921
Maprs794728921
PheGenIrs794728921
hapmaprs794728921
1000 genomesrs794728921
hgdprs794728921
ensemblrs794728921
gopubmedrs794728921
geneviewrs794728921
scholarrs794728921
googlers794728921
pharmgkbrs794728921
gwascentralrs794728921
openSNPrs794728921
23andMers794728921
23andMe allrs794728921
SNP Nexus

SNPshotrs794728921
SNPdbers794728921
MSV3drs794728921
GWAS Ctlgrs794728921
Max Magnitude0
ClinVar
Risk rs794728921(;)
Alt rs794728921(;)
Reference rs794728921(AGG;AGG)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38601919_38601921delCCT
CLNSRC
CLNACC RCV000183163.1,