Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1000778 | 1.000 | 0.040 | 11 | 61887833 | intron variant | A/G | snv | 0.59 | 3 | ||
rs10033464 | 0.807 | 0.200 | 4 | 110799605 | downstream gene variant | T/G | snv | 0.86 | 8 | ||
rs10033601 | 1.000 | 0.040 | 4 | 152330909 | intron variant | A/G | snv | 0.37 | 0.42 | 1 | |
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 | |
rs1004638 | 1.000 | 0.040 | 9 | 22115590 | intron variant | A/C;T | snv | 3 | |||
rs1007888 | 0.882 | 0.120 | 22 | 23898914 | non coding transcript exon variant | C/T | snv | 0.46 | 4 | ||
rs1008949 | 1.000 | 0.040 | 8 | 22696108 | intron variant | T/A;C;G | snv | 1 | |||
rs10093110 | 1.000 | 0.040 | 8 | 105553186 | intron variant | G/A;T | snv | 1 | |||
rs1010 | 0.807 | 0.120 | 2 | 85581859 | 3 prime UTR variant | T/C;G | snv | 7 | |||
rs10106652 | 1.000 | 0.040 | 8 | 20070649 | intergenic variant | G/A | snv | 0.29 | 3 | ||
rs10116253 | 0.851 | 0.120 | 9 | 117702042 | upstream gene variant | T/C | snv | 0.28 | 4 | ||
rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
rs10118757 | 0.827 | 0.120 | 9 | 21853340 | intron variant | A/G | snv | 0.26 | 7 | ||
rs10128951 | 1.000 | 0.040 | 12 | 124855901 | intron variant | G/A | snv | 0.47 | 1 | ||
rs10131519 | 1.000 | 0.040 | 14 | 99892957 | intron variant | T/C | snv | 0.29 | 1 | ||
rs10131894 | 1.000 | 0.040 | 14 | 74980176 | regulatory region variant | C/G | snv | 0.49 | 2 | ||
rs10139550 | 1.000 | 0.040 | 14 | 99679373 | 3 prime UTR variant | C/G | snv | 0.39 | 1 | ||
rs10159239 | 0.882 | 0.040 | 1 | 247443750 | intron variant | G/A | snv | 0.57 | 3 | ||
rs1018383 | 1.000 | 0.040 | 6 | 11784092 | intron variant | C/T | snv | 0.76 | 1 | ||
rs10186133 | 1.000 | 0.040 | 2 | 113079367 | downstream gene variant | G/A;T | snv | 1 | |||
rs1020608562 | 0.807 | 0.160 | 3 | 46373738 | missense variant | T/C | snv | 4.0E-06 | 9 | ||
rs10221742 | 1.000 | 0.040 | 2 | 21196778 | downstream gene variant | G/A | snv | 0.32 | 1 | ||
rs10237377 | 1.000 | 0.040 | 7 | 140057336 | intron variant | G/T | snv | 0.48 | 1 | ||
rs1024610 | 0.882 | 0.200 | 17 | 34253212 | upstream gene variant | T/A | snv | 0.85 | 3 | ||
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 |