Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1108143 | 1.000 | 0.080 | 2 | 234557214 | regulatory region variant | A/G | snv | 8.1E-02 | 1 | ||
rs17042407 | 1.000 | 0.080 | 2 | 112801337 | intergenic variant | T/C | snv | 0.23 | 1 | ||
rs7624041 | 1.000 | 0.080 | 3 | 94389819 | intergenic variant | G/A | snv | 0.89 | 1 | ||
rs7849280 | 1.000 | 0.080 | 9 | 133251249 | non coding transcript exon variant | A/G | snv | 1 | |||
rs372481703 | 1.000 | 0.080 | 5 | 112839106 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | |
rs80142782 | 1.000 | 0.080 | 1 | 155515236 | intron variant | T/C | snv | 2.9E-03 | 1 | ||
rs7712641 | 1.000 | 0.080 | 5 | 89607147 | intron variant | T/A;C | snv | 1 | |||
rs10029005 | 1.000 | 0.080 | 4 | 124530209 | intron variant | G/A | snv | 0.40 | 1 | ||
rs1635566 | 1.000 | 0.080 | 1 | 17356662 | intron variant | A/G | snv | 0.70 | 1 | ||
rs882537 | 1.000 | 0.080 | 1 | 17333552 | intron variant | A/G | snv | 0.64 | 1 | ||
rs10509671 | 1.000 | 0.080 | 10 | 94309297 | intron variant | T/G | snv | 0.24 | 1 | ||
rs6897169 | 1.000 | 0.080 | 5 | 40726036 | intron variant | C/A;T | snv | 0.24 | 1 | ||
rs367807476 | 1.000 | 0.080 | 19 | 1223035 | missense variant | C/G;T | snv | 9.2E-06 | 1.4E-05 | 1 | |
rs202208566 | 1.000 | 0.080 | 12 | 109903156 | missense variant | T/C | snv | 6.5E-04 | 1.7E-04 | 1 | |
rs1203145163 | 1.000 | 0.080 | 21 | 42363329 | missense variant | C/A | snv | 7.0E-06 | 1 | ||
rs11040869 | 0.925 | 0.080 | 11 | 1263382 | downstream gene variant | G/A | snv | 1.8E-02 | 2 | ||
rs11088680 | 0.925 | 0.080 | 21 | 13514758 | upstream gene variant | A/G | snv | 0.30 | 2 | ||
rs1887427 | 0.925 | 0.080 | 9 | 4979730 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
rs1892901 | 0.925 | 0.080 | 11 | 65903422 | upstream gene variant | G/A | snv | 9.5E-03 | 2 | ||
rs26160 | 0.925 | 0.080 | 5 | 145353893 | intron variant | T/C | snv | 4.5E-03 | 2 | ||
rs36012910 | 0.925 | 0.080 | 2 | 25345310 | upstream gene variant | A/C;G | snv | 2 | |||
rs4145643 | 0.925 | 0.080 | 10 | 60803097 | regulatory region variant | G/C;T | snv | 2 | |||
rs283411 | 0.925 | 0.080 | 4 | 99344800 | intron variant | C/A;T | snv | 2 | |||
rs16941667 | 0.925 | 0.080 | 12 | 111806609 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs1279599 | 0.925 | 0.080 | 6 | 110879025 | intron variant | G/A | snv | 0.87 | 2 |