Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1212415280 | 6 | 43771130 | missense variant | G/T | snv | 2.1E-05 | 2 | ||||
rs140461341 | 6 | 43782078 | missense variant | G/A | snv | 3.6E-05 | 4.2E-05 | 2 | |||
rs1201894677 | 6 | 43770833 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
rs1346131223 | 1.000 | 6 | 43777657 | missense variant | A/G | snv | 7.4E-06 | 1 | |||
rs1421145908 | 6 | 43777618 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
rs3025010 | 6 | 43779840 | non coding transcript exon variant | T/C;G | snv | 1 | |||||
rs376388064 | 6 | 43782006 | missense variant | C/T | snv | 2.8E-05 | 3.5E-05 | 1 | |||
rs541717889 | 6 | 43770888 | missense variant | G/C | snv | 2.1E-05 | 1 | ||||
rs554561071 | 6 | 43777513 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 1 | |||
rs735286 | 6 | 43776884 | non coding transcript exon variant | C/T | snv | 0.23 | 1 | ||||
rs749491856 | 1.000 | 6 | 43782071 | missense variant | A/C | snv | 1 | ||||
rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 | ||||
rs1005230 | 0.827 | 0.040 | 6 | 43768759 | upstream gene variant | T/C | snv | 0.60 | 5 | ||
rs1284410244 | 0.925 | 0.040 | 6 | 43778482 | missense variant | A/G | snv | 7.0E-06 | 4 | ||
rs138551969 | 1.000 | 0.040 | 6 | 43780749 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 4 | |
rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
rs1229919945 | 1.000 | 0.040 | 6 | 43782041 | missense variant | T/C | snv | 1 | |||
rs1404013760 | 1.000 | 0.040 | 6 | 43771137 | missense variant | G/C | snv | 8.9E-06 | 1 | ||
rs141138308 | 1.000 | 0.040 | 6 | 43780784 | missense variant | C/A;T | snv | 4.0E-06; 2.8E-05 | 1 | ||
rs1443465532 | 0.882 | 0.080 | 6 | 43774362 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs914956206 | 0.882 | 0.080 | 6 | 43770762 | missense variant | G/A;T | snv | 4 | |||
rs1305315912 | 1.000 | 0.080 | 6 | 43770736 | synonymous variant | C/T | snv | 2 | |||
rs1365501228 | 1.000 | 0.080 | 6 | 43770732 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
rs766474822 | 0.925 | 0.080 | 6 | 43770990 | missense variant | G/A | snv | 1.4E-05 | 2.1E-05 | 2 | |
rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 |