Gene | Polymorphism | Functional Consequence | Variant | Major/minor allele frequency | Hardy Weinberg p-value |
---|---|---|---|---|---|
ABCB1 | rs1045642 | Synonymous codon | A > G | 0.62/0.38 | 0.37 |
rs1128503 | Synonymous codon | A > G | 0.67/0.33 | 0.63 | |
ADRB1 | rs1801252 | Missense | A > G | 0.83/0.17 | 0.46 |
rs1801253 | Missense | G > C | 0.74/0.26 | 1 | |
CACNA1E | rs3845446 | Intron variant | T > C | 0.7/0.3 | 0.61 |
COMT | rs4633 | Synonymous codon | C > T | 0.72/0.28 | 0.86 |
rs4680 | Missense | G > A | 0.72/0.28 | 1 | |
DRD2 | rs6277 | Synonymous codon | G > A | 0.94/0.06 | 0.55 |
ESR1 | rs9340799 | Intron variant | A > G | 0.81/0.19 | 0.25 |
KCNJ6 | rs6517442 | Upstream variant | C > T | 0.73/0.27 | 0.07 |
rs2070995 | synonymous codon | T > C | 0.61/0.39 | 0.55 | |
OPRM1 | rs1799971 | Intron variant | A > G | 0.69/0.31 | 0.50 |
rs677830 | Intron variant | C > T | 0.89/0.11 | 0.46 | |
rs540825 | Intron variant | A > T | 0.92/0.08 | 1 | |
P2RX7 | rs7958311 | Intron variant | G > A | 0.52/0.48 | 0.67 |
P2RY12 | rs3732765 | Intron variant | G > A | 0.87/0.13 | 1 |
SCN11A | rs33985936 | Missense | C > T | 0.89/0.11 | 0.48 |
rs11709492 | Intron variant | C > T | 0.74/0.26 | 0.71 | |
SCN10A | rs6795970 | Missense | A > G | 0.86/0.14 | 0.38 |
SCN9A | rs6746030 | Intron variant | A > G | 0.95/0.05 | 0.36 |
rs4286289 | Intron variant | C > A | 0.56/0.44 | 1 | |
3312G > T | Missense | G > T | 0.9/0.1 | 0.69 | |
TAOK3 | rs795484 | Intron variant | T > C | 0.68/0.32 | 0.74 |
rs1277441 | Intron variant | G > A | 0.59/0.41 | 0.14 | |
TGFB1 | rs1800469 | Downstream variant | A > G | 0.51/0.49 | 0.26 |
TRPV1 | rs8065080 | Missense | T > C | 0.64/0.36 | 0.22 |
UGT2B7 | rs7439366 | Missense | T > C | 0.69/0.31 | 0.87 |
CREB1 | rs2952768 | None | T > C | 0.57/0.43 | 0.77 |