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rs794728907

From SNPedia

Orientationminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs794728907(-;-)
Make rs794728907(-;GC)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38604018
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728907
ebirs794728907
HLIrs794728907
Exacrs794728907
Varsomers794728907
Maprs794728907
PheGenIrs794728907
hapmaprs794728907
1000 genomesrs794728907
hgdprs794728907
ensemblrs794728907
gopubmedrs794728907
geneviewrs794728907
scholarrs794728907
googlers794728907
pharmgkbrs794728907
gwascentralrs794728907
openSNPrs794728907
23andMers794728907
23andMe allrs794728907
SNP Nexus

SNPshotrs794728907
SNPdbers794728907
MSV3drs794728907
GWAS Ctlgrs794728907
Max Magnitude0
ClinVar
Risk rs794728907(;)
Alt rs794728907(;)
Reference rs794728907(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38645509_38645510delGC
CLNSRC
CLNACC RCV000183146.1,