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Table 1 Observed allele frequencies for the KCNE3 sequence screened in subjects with chronic tinnitus (2N = 576).

From: Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus

SNP (dbSNP ID) chr11 position variant amino acid minor allele frequency in chronic tinnitus homozygous/heterozygous carriers of the minor allele (pHWE)
g.15,002T>C 74,168,599 T4A 0.000 -
g.15,041G>A 74,168,560 V17M 0.000 -
g.15,108C>G (rs34604640) 74,168,493 P39R 0.000 -
g.15,131C>G (rs17215444) 74,168,470 R47G 0.000 -
g.15,150G>A 74,168,451 R53H 0.000 -
g.15,190T>C (rs2270676) 74,168,411 F66F 0.125 5/62 (0.788)
g.15,220C>T (rs17221826) 74,168,381 I76I 0.000 -
g.15,240G>A (rs17215437) 74,168,361 R83H 0.005 0/3 (0.930)
g.15,255G>A (rs17221833) 74,168,346 R88H 0.000 -
g.15,288G>A 74,168,313 R99H 0.000 -
g.15,321C>T (rs11822977) 74,168,280 - 0.000 -
  1. Numbering of SNPs refers to RefSeq NG 0118331.1. Polymorphic variants in bold.