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rs794728944

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728944(-;-)
Make rs794728944(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38555726
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728944
ebirs794728944
HLIrs794728944
Exacrs794728944
Varsomers794728944
Maprs794728944
PheGenIrs794728944
hapmaprs794728944
1000 genomesrs794728944
hgdprs794728944
ensemblrs794728944
gopubmedrs794728944
geneviewrs794728944
scholarrs794728944
googlers794728944
pharmgkbrs794728944
gwascentralrs794728944
openSNPrs794728944
23andMers794728944
23andMe allrs794728944
SNP Nexus

SNPshotrs794728944
SNPdbers794728944
MSV3drs794728944
GWAS Ctlgrs794728944
Max Magnitude0
ClinVar
Risk rs794728944(;)
Alt rs794728944(;)
Reference rs794728944(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38597217delT
CLNSRC
CLNACC RCV000183206.1,