Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 10 | |
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs805303 | 0.925 | 0.160 | 6 | 31648589 | intron variant | G/A | snv | 0.45 | 5 | ||
rs11014166 | 0.882 | 0.040 | 10 | 18419869 | intron variant | A/T | snv | 0.27 | 5 | ||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 5 | |||
rs1173771 | 5 | 32814922 | regulatory region variant | A/G | snv | 0.65 | 4 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 4 | |||
rs2681472 | 0.882 | 0.080 | 12 | 89615182 | intron variant | A/G | snv | 0.14 | 4 | ||
rs1378942 | 0.790 | 0.240 | 15 | 74785026 | intron variant | C/A;T | snv | 4 | |||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 4 | |||||
rs932764 | 10 | 94136183 | intron variant | A/G | snv | 0.38 | 4 | ||||
rs6015450 | 20 | 59176062 | intron variant | A/G | snv | 0.14 | 4 | ||||
rs11953630 | 5 | 158418394 | intergenic variant | C/A;T | snv | 3 | |||||
rs1327235 | 20 | 10988382 | intron variant | A/G | snv | 0.46 | 3 | ||||
rs1458038 | 0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 | 3 | ||
rs16998073 | 0.925 | 0.120 | 4 | 80263187 | upstream gene variant | A/G;T | snv | 3 | |||
rs4373814 | 10 | 18131043 | intergenic variant | G/C;T | snv | 3 | |||||
rs6495122 | 1.000 | 0.040 | 15 | 74833304 | downstream gene variant | A/C | snv | 0.44 | 3 | ||
rs7129220 | 11 | 10328991 | intron variant | G/A | snv | 0.10 | 3 | ||||
rs1530440 | 1.000 | 0.040 | 10 | 61764833 | intron variant | C/T | snv | 0.15 | 3 | ||
rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 3 | ||
rs419076 | 3 | 169383098 | intron variant | T/A;C | snv | 3 | |||||
rs9815354 | 0.925 | 0.160 | 3 | 41871159 | intron variant | G/A;T | snv | 3 |