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rs794728865

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728865(C;T)
Make rs794728865(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585903
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728865
ebirs794728865
HLIrs794728865
Exacrs794728865
Varsomers794728865
Maprs794728865
PheGenIrs794728865
hapmaprs794728865
1000 genomesrs794728865
hgdprs794728865
ensemblrs794728865
gopubmedrs794728865
geneviewrs794728865
scholarrs794728865
googlers794728865
pharmgkbrs794728865
gwascentralrs794728865
openSNPrs794728865
23andMers794728865
23andMe allrs794728865
SNP Nexus

SNPshotrs794728865
SNPdbers794728865
MSV3drs794728865
GWAS Ctlgrs794728865
Max Magnitude0
ClinVar
Risk rs794728865(T;T)
Alt rs794728865(T;T)
Reference rs794728865(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38627394G>A
CLNSRC
CLNACC RCV000183005.2,