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Table 2 General information of selected SNPs and Hardy–Weinberg test

From: A missense variant rs2585405 in clock gene PER1 is associated with the increased risk of noise-induced hearing loss in a Chinese occupational population

Gene SNP Alleles Chromosome Functional Consequence MAF databasea P for HWEb
PER1 rs2253820 A/G 17:8144851 splice region variant 0.44 0.954
  rs2585405 C/G 17:8143454 missense variant 0.23 0.441
PER2 rs56386336 A/G 2:238245307 3'prime UTR variant 0.09 1.000
  rs934945 A/G 2:238246412 missense variant 0.17 0.026
CRY1 rs1056560 G/T 12:106991832 3'prime UTR variant 0.47 0.402
  rs3809236 C/T 12:107093269 5'prime UTR variant 0.20 0.892
CRY2 rs2292910 C/A 11:45882062 3'prime UTR variant 0.42 0.994
  rs6798 C/T 11:45882926 3'prime UTR variant 0.24 0.892
BDNF rs11030099 A/C 11:27656036 3'prime UTR variant 0.23 0.205
  rs7124442 C/T 11:27655494 3'prime UTR variant 0.33 0.654
  rs6265 A/G 11:27658369 missense variant 0.20 0.264
NTF3 rs1805149 A/G 12:5494441 missense variant 0.12 0.592
  1. aData from NCBI dbSNP
  2. bP value of Hardy–Weinberg test