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rs11708996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs11708996(C;C)
Make rs11708996(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38592432
GeneSCN5A
is asnp
is mentioned by
dbSNPrs11708996
ebirs11708996
HLIrs11708996
Exacrs11708996
Varsomers11708996
Maprs11708996
PheGenIrs11708996
hapmaprs11708996
1000 genomesrs11708996
hgdprs11708996
ensemblrs11708996
gopubmedrs11708996
geneviewrs11708996
scholarrs11708996
googlers11708996
pharmgkbrs11708996
gwascentralrs11708996
openSNPrs11708996
23andMers11708996
23andMe allrs11708996
SNP Nexus

SNPshotrs11708996
SNPdbers11708996
MSV3drs11708996
GWAS Ctlgrs11708996
GMAF0.08999
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20062060OA-icon.png]
Trait PR interval
Title Genome-wide association study of PR interval.
Risk Allele C
P-val 6E-26
Odds Ratio 3.04 [2.47-3.61] ms increase
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele C
P-val 0.000007
Odds Ratio 0.4700 [NR] ms increase


[PMID 21347284OA-icon.png] Genome-wide association studies of the PR interval in African Americans.

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 1E-14
Odds Ratio 1.73 [1.51-1.99]