Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1001179 | 0.641 | 0.680 | 11 | 34438684 | upstream gene variant | C/T | snv | 0.16 | 33 | ||
rs10012 | 0.716 | 0.280 | 2 | 38075247 | missense variant | G/C | snv | 0.31 | 0.36 | 16 | |
rs1004072779 | 0.925 | 0.080 | 21 | 38403547 | missense variant | T/C | snv | 2.1E-05 | 2 | ||
rs10046 | 0.708 | 0.400 | 15 | 51210789 | 3 prime UTR variant | G/A | snv | 0.45 | 0.43 | 18 | |
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 53 | ||
rs10090154 | 0.807 | 0.160 | 8 | 127519892 | intergenic variant | T/A;C | snv | 7 | |||
rs1012477 | 0.827 | 0.160 | 1 | 7798075 | intron variant | G/C | snv | 0.16 | 8 | ||
rs1016343 | 0.807 | 0.240 | 8 | 127081052 | non coding transcript exon variant | C/T | snv | 0.20 | 8 | ||
rs10165970 | 0.708 | 0.320 | 2 | 100840527 | intron variant | G/A | snv | 0.16 | 18 | ||
rs10175368 | 0.925 | 0.080 | 2 | 38080719 | intron variant | C/T | snv | 0.23 | 4 | ||
rs10187424 | 0.925 | 0.080 | 2 | 85567174 | intron variant | T/A;C | snv | 2 | |||
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
rs103294 | 0.827 | 0.200 | 19 | 54293995 | downstream gene variant | T/C | snv | 0.82 | 7 | ||
rs1034528 | 0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 | 5 | ||
rs1034866440 | 0.851 | 0.160 | X | 67643401 | missense variant | G/A | snv | 5.7E-06 | 4 | ||
rs1041258260 | 0.925 | 0.080 | 19 | 43552170 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1042489 | 0.851 | 0.160 | 17 | 78224125 | 3 prime UTR variant | T/C | snv | 0.40 | 5 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs10426628 | 0.925 | 0.080 | 19 | 48589173 | intron variant | A/G | snv | 0.78 | 2 | ||
rs10432782 | 0.807 | 0.160 | 21 | 31664078 | intron variant | T/G | snv | 0.19 | 7 | ||
rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
rs1045531 | 0.882 | 0.080 | 8 | 142682129 | synonymous variant | C/A | snv | 0.45 | 0.44 | 3 | |
rs10459592 | 0.925 | 0.080 | 15 | 51243944 | intron variant | T/G | snv | 0.49 | 2 | ||
rs1046040 | 0.925 | 0.080 | 19 | 1095515 | upstream gene variant | G/A | snv | 0.21 | 2 |