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rs879293

From SNPedia

Orientationminus
Stabilizedminus
Make rs879293(A;A)
Make rs879293(A;G)
Make rs879293(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position42197628
GenePLAT
is asnp
is mentioned by
dbSNPrs879293
ebirs879293
HLIrs879293
Exacrs879293
Varsomers879293
Maprs879293
PheGenIrs879293
hapmaprs879293
1000 genomesrs879293
hgdprs879293
ensemblrs879293
gopubmedrs879293
geneviewrs879293
scholarrs879293
googlers879293
pharmgkbrs879293
gwascentralrs879293
openSNPrs879293
23andMers879293
23andMe allrs879293
SNP Nexus

SNPshotrs879293
SNPdbers879293
MSV3drs879293
GWAS Ctlgrs879293
GMAF0.3535
Max Magnitude
? (A;A) (A;G) (G;G) 28
A study of maternal and fetal DNA from 370 US Caucasian birth-events (172 cases and 198 controls) concluded that the single strongest effect observed in maternal DNA was for SNP rs879293, with a significant allelic (p = 2.30x10e-3) and genotypic association (p = 2.0x10e-6) with spontaneous preterm birth (PTB). The odds ratio for this SNP was 2.80 (CI:1.77-4.44) under a recessive model. [PMID 18818748OA-icon.png]


[PMID 18787196OA-icon.png] Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study.