Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs762471803 | 0.925 | 0.040 | 11 | 102114201 | missense variant | T/G | snv | 6 | |||
rs761872690 | 0.925 | 0.080 | 11 | 101128246 | synonymous variant | G/A | snv | 2.8E-05 | 3 | ||
rs760043106 | 0.645 | 0.440 | 17 | 7674947 | missense variant | A/C;G;T | snv | 32 | |||
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 21 | ||
rs759478535 | 0.851 | 0.080 | 17 | 39708351 | missense variant | A/G | snv | 6.8E-05 | 4.2E-05 | 6 | |
rs759435862 | 0.925 | 0.080 | 2 | 8776852 | missense variant | C/A;T | snv | 2.0E-05 | 5 | ||
rs758272654 | 0.611 | 0.680 | 20 | 58909201 | synonymous variant | T/C | snv | 4.0E-06 | 7.0E-06 | 50 | |
rs756160717 | 3 | 12585204 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 1 | |||
rs7553007 | 0.827 | 0.120 | 1 | 159728759 | intergenic variant | G/A | snv | 0.31 | 7 | ||
rs754854286 | 1.000 | 0.120 | 10 | 31520432 | missense variant | G/C | snv | 3 | |||
rs753066745 | X | 81277164 | missense variant | C/T | snv | 1.7E-05 | 9.5E-06 | 2 | |||
rs752021744 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 29 | ||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 24 | ||
rs746429 | 0.882 | 0.120 | 11 | 65649963 | synonymous variant | G/A | snv | 0.31 | 0.30 | 8 | |
rs7371084 | 0.925 | 0.120 | 2 | 48712814 | intron variant | T/C | snv | 0.12 | 3 | ||
rs735482 | 0.742 | 0.160 | 19 | 45408744 | missense variant | A/C | snv | 0.21 | 0.20 | 16 | |
rs730882002 | 0.925 | 0.040 | 17 | 7674956 | missense variant | T/C | snv | 6 | |||
rs723526 | 1.000 | 7 | 55067126 | intron variant | A/G | snv | 0.86 | 2 | |||
rs71310379 | 3 | 179199003 | missense variant | C/A | snv | 4.4E-05 | 4.2E-05 | 1 | |||
rs712 | 0.677 | 0.360 | 12 | 25209618 | 3 prime UTR variant | A/C | snv | 0.46 | 24 | ||
rs7034162 | 0.882 | 0.040 | 9 | 14190288 | intron variant | A/T | snv | 0.81 | 4 | ||
rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
rs6983561 | 0.925 | 0.080 | 8 | 127094635 | intron variant | A/C | snv | 0.17 | 3 | ||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 62 | ||
rs6973569 | 0.851 | 0.080 | 7 | 34583412 | intron variant | G/A | snv | 4.7E-02 | 5 |