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rs794728906

From SNPedia

Orientationminus
Geno Mag Summary
(CAAG;CAAG) 0 common in clinvar
Make rs794728906(-;-)
Make rs794728906(-;CAAG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38604816
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728906
ebirs794728906
HLIrs794728906
Exacrs794728906
Varsomers794728906
Maprs794728906
PheGenIrs794728906
hapmaprs794728906
1000 genomesrs794728906
hgdprs794728906
ensemblrs794728906
gopubmedrs794728906
geneviewrs794728906
scholarrs794728906
googlers794728906
pharmgkbrs794728906
gwascentralrs794728906
openSNPrs794728906
23andMers794728906
23andMe allrs794728906
SNP Nexus

SNPshotrs794728906
SNPdbers794728906
MSV3drs794728906
GWAS Ctlgrs794728906
Max Magnitude0
ClinVar
Risk rs794728906(;)
Alt rs794728906(;)
Reference rs794728906(CAAG;CAAG)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38646307_38646310delCTTG
CLNSRC
CLNACC RCV000183145.2,