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. 2017 Jul;57(1):35–46. doi: 10.1165/rcmb.2016-0331OC

Table 4.

Genetic Risk Score Loci

Gene SNP Identifier
CHRNA3 rs12914385
RAB4B/EGLN2/MIA/CYP2A6 rs7937
RIN3 rs754388
TGFB2 rs4846480
MMP12 rs626750
HHIP rs13141641
FAM13A rs4416442
PTCH1 rs16909898
C10orf11 rs11001819
HTR4 rs11168048
DNER rs7594321
HDAC4-FLJ43879 rs12477314
MFAP2 rs2284746
ARMC2 rs2798641
LRP1 rs11172113
RARB rs1529672
GSTCD/INTS12/NPNT rs10516526
NCR3-AIF1 rs2857595
MECOM/EVI1 rs1344555
AGER/PPT2 rs2070600
ZKSCAN3 rs6903823
SPATA9-RHOBTB3 rs153916
MMP15 rs12447804
HLA-DQB1 rs7765379
KCNJ2/CASC17 rs11654749
GPR126 rs3817928
TGFB2-LYPLAL1 rs993925
CDC123 rs7068966
KCNE2-LINC00310/C21orf82 rs9978142
THSD4 rs12899618

Definition of abbreviations: COPD7, genetic risk score composed of seven COPD risk SNPs (ranging from 0 to 14 scoring alleles); LUNG30, genetic risk score compsed of thirty lung function associated risk SNPs (ranging from 0 to 60 scoring alleles); SNP, single-nucleotide polymorphism.

Genetic risk scores were composed using previous chronic obstructive pulmonary disease (COPD) and lung function–associated loci. The LUNG30 score included all of the loci listed in the above table; the COPD7 score included only those in the bold. Loci names are based on previously reported SNP associations annotated to the nearest gene or region.