rs17121510

Orientation

plus

Stabilized

plus

Make rs17121510(A;A)

Make rs17121510(A;G)

Make rs17121510(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

118005440

Gene	LOC107984395

is a	snp
is	mentioned by
dbSNP	rs17121510
dbSNP (classic)	rs17121510
ClinGen	rs17121510
ebi	rs17121510
HLI	rs17121510
Exac	rs17121510
Gnomad	rs17121510
Varsome	rs17121510
LitVar	rs17121510
Map	rs17121510
PheGenI	rs17121510
Biobank	rs17121510
1000 genomes	rs17121510
hgdp	rs17121510
ensembl	rs17121510
geneview	rs17121510
scholar	rs17121510
google	rs17121510
pharmgkb	rs17121510
gwascentral	rs17121510
openSNP	rs17121510
23andMe	rs17121510
SNPshot	rs17121510
SNPdbe	rs17121510
MSV3d	rs17121510
GWAS Ctlg	rs17121510

GMAF

0.1446

Max Magnitude

0

?	(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 in fetal DNA was associated with rs17121510 in the interleukin-10 receptor antagonist (IL-10RA) gene at both allelic (p = 0.01) and genotypic (p = 3.34x10e-4) levels. The odds ratio for preterm birth for the genotypic additive model was 1.92 (CI: 1.15-3.19, p = 2.00x10e-3). [PMID 18818748]

[PMID 20463618] Role of polymorphic variants as genetic modulators of infection in neonatal sepsis.