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rs12567209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12567209(A;A)
Make rs12567209(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position162066689
is asnp
is mentioned by
dbSNPrs12567209
ebirs12567209
HLIrs12567209
Exacrs12567209
Varsomers12567209
Maprs12567209
PheGenIrs12567209
hapmaprs12567209
1000 genomesrs12567209
hgdprs12567209
ensemblrs12567209
gopubmedrs12567209
geneviewrs12567209
scholarrs12567209
googlers12567209
pharmgkbrs12567209
gwascentralrs12567209
openSNPrs12567209
23andMers12567209
23andMe allrs12567209
SNP Nexus

SNPshotrs12567209
SNPdbers12567209
MSV3drs12567209
GWAS Ctlgrs12567209
GMAF0.1107
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19204306OA-icon.png] rs10494366, rs4657139 and rs16847548 were significantly associated with adjusted QT interval in whites. relative hazard of SCD associated with each C allele at rs16847548 was 1.31. rs12567209 was also independently associated with SCD in whites (relative hazard 0.57, 95% confidence interval 0.39 to 0.83, P=0.003). No significant associations observed in blacks.

[PMID 19180230OA-icon.png] Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.

[PMID 19643915OA-icon.png] Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.