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rs10428132

From SNPedia

Orientationplus
Stabilizedplus
Make rs10428132(G;G)
Make rs10428132(G;T)
Make rs10428132(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38736063
GeneSCN10A
is asnp
is mentioned by
dbSNPrs10428132
ebirs10428132
HLIrs10428132
Exacrs10428132
Varsomers10428132
Maprs10428132
PheGenIrs10428132
hapmaprs10428132
1000 genomesrs10428132
hgdprs10428132
ensemblrs10428132
gopubmedrs10428132
geneviewrs10428132
scholarrs10428132
googlers10428132
pharmgkbrs10428132
gwascentralrs10428132
openSNPrs10428132
23andMers10428132
23andMe allrs10428132
SNP Nexus

SNPshotrs10428132
SNPdbers10428132
MSV3drs10428132
GWAS Ctlgrs10428132
GMAF0.2957
Max Magnitude
? (G;G) (G;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 T
P-val 1E-68
Odds Ratio 2.55 [2.30-2.84]