Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs8099917 | 0.581 | 0.600 | 19 | 39252525 | upstream gene variant | T/G | snv | 0.16 | 60 | ||
rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
rs8177374 | 0.672 | 0.520 | 11 | 126292948 | missense variant | C/T | snv | 0.12 | 0.11 | 22 | |
rs3765524 | 0.724 | 0.320 | 10 | 94298541 | missense variant | C/T | snv | 0.27 | 0.31 | 17 | |
rs4804803 | 0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 | 15 | ||
rs1800875 | 0.742 | 0.360 | 14 | 24510132 | upstream gene variant | C/T | snv | 0.41 | 12 | ||
rs762513613 | 0.752 | 0.280 | 1 | 161591315 | missense variant | A/G | snv | 4.2E-06 | 7.4E-06 | 11 | |
rs3740360 | 0.827 | 0.240 | 10 | 94265734 | intron variant | A/C | snv | 9.7E-02 | 8.4E-02 | 7 | |
rs3132468 | 0.827 | 0.240 | 6 | 31507709 | intron variant | C/T | snv | 0.77 | 5 | ||
rs5745568 | 0.882 | 0.080 | 6 | 33580617 | intron variant | G/T | snv | 0.19 | 4 | ||
rs750898115 | 0.882 | 0.080 | 4 | 75787191 | missense variant | A/G | snv | 1.0E-05 | 3.5E-05 | 4 | |
rs1285933 | 0.925 | 0.040 | 7 | 141927349 | intron variant | G/A | snv | 0.54 | 2 | ||
rs1447043692 | 0.925 | 0.040 | 10 | 98641918 | missense variant | C/T | snv | 2 | |||
rs3739319 | 0.925 | 0.040 | 8 | 39927802 | intron variant | G/A | snv | 0.40 | 0.37 | 2 | |
rs371057322 | 0.925 | 0.040 | 2 | 8793960 | missense variant | T/C | snv | 1.4E-05 | 2 | ||
rs6500818 | 0.925 | 0.040 | 16 | 6767374 | intron variant | C/T | snv | 0.11 | 2 | ||
rs10104997 | 0.925 | 0.040 | 8 | 54527508 | intron variant | C/T | snv | 0.19 | 2 | ||
rs4973 | 1.000 | 0.040 | 17 | 63486691 | synonymous variant | A/G | snv | 1 | |||
rs1317403430 | 1.000 | 0.040 | 1 | 196673869 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs2780831 | 1.000 | 0.040 | 1 | 64880504 | intron variant | C/T | snv | 0.35 | 1 |