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rs794728900

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728900(A;A)
Make rs794728900(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550746
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728900
ebirs794728900
HLIrs794728900
Exacrs794728900
Varsomers794728900
Maprs794728900
PheGenIrs794728900
hapmaprs794728900
1000 genomesrs794728900
hgdprs794728900
ensemblrs794728900
gopubmedrs794728900
geneviewrs794728900
scholarrs794728900
googlers794728900
pharmgkbrs794728900
gwascentralrs794728900
openSNPrs794728900
23andMers794728900
23andMe allrs794728900
SNP Nexus

SNPshotrs794728900
SNPdbers794728900
MSV3drs794728900
GWAS Ctlgrs794728900
Max Magnitude0
ClinVar
Risk rs794728900(A;A)
Alt rs794728900(A;A)
Reference rs794728900(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592237C>T
CLNSRC
CLNACC RCV000183129.2,