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 | - |