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rs6800541

From SNPedia

Orientationplus
Stabilizedplus
Make rs6800541(C;C)
Make rs6800541(C;T)
Make rs6800541(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38733341
GeneSCN10A
is asnp
is mentioned by
dbSNPrs6800541
ebirs6800541
HLIrs6800541
Exacrs6800541
Varsomers6800541
Maprs6800541
PheGenIrs6800541
hapmaprs6800541
1000 genomesrs6800541
hgdprs6800541
ensemblrs6800541
gopubmedrs6800541
geneviewrs6800541
scholarrs6800541
googlers6800541
pharmgkbrs6800541
gwascentralrs6800541
openSNPrs6800541
23andMers6800541
23andMe allrs6800541
SNP Nexus

SNPshotrs6800541
SNPdbers6800541
MSV3drs6800541
GWAS Ctlgrs6800541
GMAF0.259
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20062060OA-icon.png]
Trait PR interval
Title Genome-wide association study of PR interval
Risk Allele C
P-val 2E-74
Odds Ratio 3.77 [3.37-4.17] ms increase
GWAS snp
PMID [PMID 21041692OA-icon.png]
Trait
Title Identification of Genomic Predictors of Atrioventricular Conduction. Using Electronic Medical Records as a Tool for Genome Science
Risk Allele C
P-val 5E-7
Odds Ratio 2.6000 [1.62-3.70] ms increase


[PMID 23092954OA-icon.png] SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.


[PMID 25085921] Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation


[PMID 25691686] Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation