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Table 3 Independent loci reaching statistical significance false discovery rate shared between cataracts and hearing difficulties in the hg19 human genome reference

From: Epidemiologic association and shared genetic architecture between cataract and hearing difficulties among middle-aged and older adults

SNP

Chr

Pos

Nearest gene

Alleles

A1/A2

MAF

Cond/conjFDR

rs9290737

3

181,979,272

LINC01206

A/G

0.32

6.08E-05

rs4709714

6

163,801,031

QKI

C/T

0.56

6.97E-05

rs55728135

7

43,692,493

STK17A

A/G

0.21

7.76E-05

rs12295166

11

88,976,157

TYR

T/C

0.37

7.81E-05

rs9912530

17

44,836,302

NSF

T/C

0.71

9.82E-05

rs613872

18

53,210,302

TCF4

G/T

0.83

0.000187727

  1. Note: Gene context for each significant independent SNP was examined in the NCBI database (http://www.ncbi.nlm.nih.gov/). Abbreviations: SNP, single nucleotide polymorphism; MAF, minor allele frequency; Cond/conjFDR, conditional/conjunctional false discovery rate
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Human Genomics

ISSN: 1479-7364