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rs9388451

From SNPedia

Orientationplus
Stabilizedplus
Make rs9388451(C;C)
Make rs9388451(C;T)
Make rs9388451(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position125769231
is asnp
is mentioned by
dbSNPrs9388451
ebirs9388451
HLIrs9388451
Exacrs9388451
Varsomers9388451
Maprs9388451
PheGenIrs9388451
hapmaprs9388451
1000 genomesrs9388451
hgdprs9388451
ensemblrs9388451
gopubmedrs9388451
geneviewrs9388451
scholarrs9388451
googlers9388451
pharmgkbrs9388451
gwascentralrs9388451
openSNPrs9388451
23andMers9388451
23andMe allrs9388451
SNP Nexus

SNPshotrs9388451
SNPdbers9388451
MSV3drs9388451
GWAS Ctlgrs9388451
GMAF0.4605
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23872634OA-icon.png]
Trait Brugada syndrome
Title Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Risk Allele C
P-val 5E-17
Odds Ratio 1.58 [1.42-1.75]