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rs794728936

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728936(A;A)
Make rs794728936(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38556540
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728936
ebirs794728936
HLIrs794728936
Exacrs794728936
Varsomers794728936
Maprs794728936
PheGenIrs794728936
hapmaprs794728936
1000 genomesrs794728936
hgdprs794728936
ensemblrs794728936
gopubmedrs794728936
geneviewrs794728936
scholarrs794728936
googlers794728936
pharmgkbrs794728936
gwascentralrs794728936
openSNPrs794728936
23andMers794728936
23andMe allrs794728936
SNP Nexus

SNPshotrs794728936
SNPdbers794728936
MSV3drs794728936
GWAS Ctlgrs794728936
Max Magnitude0
ClinVar
Risk rs794728936(A;A)
Alt rs794728936(A;A)
Reference rs794728936(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38598031C>T
CLNSRC
CLNACC RCV000183192.2,