Clinical Study

Association of a FGFR-4 Gene Polymorphism with Bronchopulmonary Dysplasia and Neonatal Respiratory Distress

Table 1

Studied polymorphisms. Genotyped polymorphisms, their corresponding reference SNP ID number, nucleotide substitution, and gene region. SNPs in exon regions are indicated as their amino acid substitution.

GenePolymorphismAllelesGene region

MMP-1 rs1799750G/GGPromotor
rs7125062C/TIntron

MMP-2 rs7201A/C3′UTR
rs243865C/TPromotor
rs17301608C/TIntron

MMP-9 rs20544C/T3′UTR
rs3918242C/TPromoter
rs17576A/G279 Gln/Arg

MMP-12 rs2276109A/GPromoter
rs652438A/G357 Asn/Ser

MMP-16 rs2664352C/TIntron

FGFR-2 rs2981579A/GIntron
rs1219648A/GIntron

FGFR-4 rs376618A/G136 Leu/Pro
rs1966265A/G10 Ile/Val

FGF-2 rs11938826C/GIntron

FGF-3 rs11263591G/CIntron
rs10796856T/CIntron

FGF-4 rs3740639 C/T3′UTR

FGF-7 rs16962440C/TIntron

FGF-7, C15 or f33 rs4316697 G/AIntron
rs10519230C/GIntron

FGF-18 rs4559013G/AIntron

SIRPA rs3828016A/GIntron
rs4814734A/TIntron

TTF-1 rs11628131A/CPromoter
rs999460C/TDownstream