Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10013040 | 1.000 | 0.080 | 4 | 177309998 | synonymous variant | C/A | snv | 0.20 | 0.20 | 1 | |
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 | |
rs1007888 | 0.882 | 0.120 | 22 | 23898914 | non coding transcript exon variant | C/T | snv | 0.46 | 4 | ||
rs1008563 | 1.000 | 0.080 | 2 | 218162165 | downstream gene variant | G/A | snv | 0.43 | 1 | ||
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 | ||
rs1012841819 | 0.882 | 0.160 | 2 | 96115728 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs10176176 | 1.000 | 0.080 | 2 | 85534925 | upstream gene variant | A/T | snv | 0.54 | 1 | ||
rs1024323 | 0.882 | 0.160 | 4 | 3004316 | missense variant | C/A;G;T | snv | 0.36 | 4 | ||
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
rs10263017 | 1.000 | 0.080 | 7 | 6026173 | intron variant | G/C;T | snv | 1 | |||
rs10281500 | 1.000 | 0.080 | 7 | 55475197 | intron variant | C/G | snv | 0.32 | 1 | ||
rs10304 | 0.925 | 0.120 | 22 | 31104550 | 3 prime UTR variant | G/A | snv | 0.12 | 2 | ||
rs1041740 | 0.807 | 0.320 | 21 | 31667849 | intron variant | C/T | snv | 0.24 | 8 | ||
rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 25 | |
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 15 | |
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042579 | 0.732 | 0.240 | 20 | 23048087 | missense variant | G/A;T | snv | 0.19 | 16 | ||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs10432782 | 0.807 | 0.160 | 21 | 31664078 | intron variant | T/G | snv | 0.19 | 7 | ||
rs1045274 | 1.000 | 0.080 | 16 | 580902 | synonymous variant | C/G;T | snv | 0.16; 2.0E-05 | 1 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 33 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs104895285 | 1.000 | 0.080 | 12 | 6330873 | missense variant | A/T | snv | 1 |