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Table 3 Summary of NFE2L2 variants associated with acute respiratory distress syndrome susceptibility with false discovery rate <0.05

From: Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis

Positiona

SNPs

Functionalityb

Minor allele

MAF

R 2

OR (95 % CI)

p value

177,265,308

rs6721961

5′ flanking

T

0.111

0.32

1.93 (1.17–3.18)

0.0089

Histone mark, DHS

177,255,662

rs10188193

Intron 1

T

0.110

0.33

1.95 (1.19–3.17)

0.0071

177,255,583

rs10188107

Intron 1

T

0.110

0.33

1.95 (1.19–3.17)

0.0071

177,254,567

rs10497511

Intron 1

G

0.110

0.33

1.95 (1.19–3.17)

0.0070

DHS

177,253,821

rs2001297

Intron 1

C

0.110

0.33

1.95 (1.20–3.16)

0.0069

Histone mark

177,253,036

rs4243387c

Intron 1

C

0.112

0.34

1.93 (1.19–3.12)

0.0068

Histone mark

177,249,903

rs10930781c

Intron 1

A

0.106

0.35

1.90 (1.17–3.12)

0.0085

177,248,755

rs1962142c

Intron 1

A

0.103

0.33

1.96 (1.18–3.23)

0.0083

Histone mark

177,240,415

rs2364720

Intron 1

A

0.106

0.35

1.90 (1.17–3.09)

0.0082

Histone mark

177,235,696

rs2001350c

Intron 1

C

0.103

0.32

2.00 (1.20–3.35)

0.0075

Histone mark

  1. CI confidence interval, DHS DNase I hypersensitivity site, FDR false discovery rate, MAF minor allele frequency, OR odds ratio, R 2 squared correlation between imputed and observed genotypes, SNP single-nucleotide polymorphism
  2. aAccording to National Center for Biotechnology Genome Reference Consortium NCBI build GRCh38
  3. bFunctionality obtained from HaploReg v3 [27]
  4. cSNPs associated with primary graft dysfunction in Cantu et al. [11]