Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 27 | ||
rs12579302 | 0.851 | 0.120 | 12 | 89656726 | intron variant | A/G | snv | 0.15 | 19 | ||
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 18 | ||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs7137828 | 0.763 | 0.200 | 12 | 111494996 | intron variant | C/A;T | snv | 15 | |||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs3918226 | 0.925 | 0.080 | 7 | 150993088 | intron variant | C/T | snv | 5.7E-02 | 12 | ||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 10 | |||
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 10 | |||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 9 | ||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 8 | ||||
rs740746 | 10 | 114033028 | intergenic variant | G/A | snv | 0.70 | 8 | ||||
rs2306363 | 11 | 65638129 | 5 prime UTR variant | G/T | snv | 0.15 | 7 | ||||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs11099097 | 4 | 80246155 | intergenic variant | C/T | snv | 0.30 | 6 | ||||
rs1290784 | 3 | 169379112 | intron variant | C/A;T | snv | 6 | |||||
rs13125101 | 4 | 80253438 | TF binding site variant | G/A | snv | 0.24 | 6 |