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rs397517956

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517956(A;A)
Make rs397517956(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38550512
GeneSCN5A
is asnp
is mentioned by
dbSNPrs397517956
ebirs397517956
HLIrs397517956
Exacrs397517956
Varsomers397517956
Maprs397517956
PheGenIrs397517956
hapmaprs397517956
1000 genomesrs397517956
hgdprs397517956
ensemblrs397517956
gopubmedrs397517956
geneviewrs397517956
scholarrs397517956
googlers397517956
pharmgkbrs397517956
gwascentralrs397517956
openSNPrs397517956
23andMers397517956
23andMe allrs397517956
SNP Nexus

SNPshotrs397517956
SNPdbers397517956
MSV3drs397517956
GWAS Ctlgrs397517956
Max Magnitude0
ClinVar
Risk rs397517956(A;A)
Alt rs397517956(A;A)
Reference rs397517956(G;G)
Significance Probable-Pathogenic
Disease not specified Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not specified Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592003C>T
CLNSRC
CLNACC RCV000041633.3, RCV000231684.1,