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rs10850409

From SNPedia

Orientationplus
Stabilizedplus
Make rs10850409(A;A)
Make rs10850409(A;G)
Make rs10850409(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position114943935
is asnp
is mentioned by
dbSNPrs10850409
ebirs10850409
HLIrs10850409
Exacrs10850409
Varsomers10850409
Maprs10850409
PheGenIrs10850409
hapmaprs10850409
1000 genomesrs10850409
hgdprs10850409
ensemblrs10850409
gopubmedrs10850409
geneviewrs10850409
scholarrs10850409
googlers10850409
pharmgkbrs10850409
gwascentralrs10850409
openSNPrs10850409
23andMers10850409
23andMe allrs10850409
SNP Nexus

SNPshotrs10850409
SNPdbers10850409
MSV3drs10850409
GWAS Ctlgrs10850409
GMAF0.3572
Max Magnitude
? (A;A) (A;G) (G;G) 28
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 A
P-val 3E-10
Odds Ratio 0.4900 [0.33-0.65] ms decrease
GWAS snp
PMID [PMID 24850809OA-icon.png]
Trait PR segment
Title Genetic determinants of P wave duration and PR segment.
Risk Allele A
P-val 8E-13
Odds Ratio 1.65 [1.20-2.10] unit increase