| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10167914 | 1.000 | 0.040 | 2 | 112805784 | TF binding site variant | A/G | snv | 0.31 | 1 | ||
| rs10282436 | 1.000 | 0.040 | 7 | 25833490 | upstream gene variant | G/T | snv | 0.19 | 1 | ||
| rs10419023 | 1.000 | 0.040 | 19 | 48427965 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs10508881 | 1.000 | 0.040 | 10 | 44046117 | regulatory region variant | A/G | snv | 0.50 | 1 | ||
| rs1065780 | 1.000 | 0.040 | 7 | 45888078 | upstream gene variant | G/A | snv | 0.39 | 1 | ||
| rs10777670 | 1.000 | 0.040 | 12 | 95181055 | intron variant | G/A | snv | 0.23 | 1 | ||
| rs10794288 | 1.000 | 0.040 | 11 | 1086825 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs10859856 | 1.000 | 0.040 | 12 | 95237500 | intron variant | T/C | snv | 0.48 | 1 | ||
| rs10953316 | 1.000 | 0.040 | 7 | 101038481 | synonymous variant | A/C;G;T | snv | 8.0E-06; 0.64 | 1 | ||
| rs10965235 | 1.000 | 0.040 | 9 | 22115106 | intron variant | C/A | snv | 0.15 | 1 | ||
| rs10975519 | 1.000 | 0.040 | 9 | 6253571 | synonymous variant | C/T | snv | 0.38 | 0.35 | 1 | |
| rs1104760 | 1.000 | 0.040 | 3 | 195790450 | missense variant | G/A;T | snv | 0.78; 2.8E-05 | 1 | ||
| rs11085835 | 1.000 | 0.040 | 19 | 13221196 | intron variant | T/A;C | snv | 1 | |||
| rs11132055 | 1.000 | 0.040 | 4 | 181401652 | intergenic variant | T/A;G | snv | 1 | |||
| rs11245954 | 1.000 | 0.040 | 11 | 1107170 | non coding transcript exon variant | A/G | snv | 6.7E-02 | 8.9E-02 | 1 | |
| rs113850637 | 1.000 | 0.040 | 3 | 104131556 | intergenic variant | C/T | snv | 0.14 | 1 | ||
| rs1159327 | 1.000 | 0.040 | 6 | 151726887 | intron variant | C/T | snv | 0.32 | 1 | ||
| rs116175374 | 1.000 | 0.040 | 2 | 31202319 | intron variant | G/A | snv | 4.9E-02 | 1 | ||
| rs116250606 | 1.000 | 0.040 | 10 | 103473496 | missense variant | C/T | snv | 6.5E-06; 4.1E-03 | 2.3E-02 | 1 | |
| rs11674184 | 1.000 | 0.040 | 2 | 11581409 | intron variant | T/A;G | snv | 1 | |||
| rs11692361 | 1.000 | 0.040 | 2 | 66496567 | intron variant | C/G;T | snv | 1 | |||
| rs11977660 | 1.000 | 0.040 | 7 | 55094643 | intron variant | T/C | snv | 0.42 | 1 | ||
| rs1203495492 | 1.000 | 0.040 | 20 | 63408489 | missense variant | C/T | snv | 2.1E-05 | 1 | ||
| rs12449465 | 1.000 | 0.040 | 17 | 3126260 | downstream gene variant | T/A;C | snv | 1 | |||
| rs13394619 | 1.000 | 0.040 | 2 | 11587381 | splice acceptor variant | G/A | snv | 0.53 | 0.61 | 1 |