Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6651252 | 0.790 | 0.200 | 8 | 128554935 | intron variant | T/C | snv | 0.19 | 8 | ||
rs17293632 | 0.763 | 0.240 | 15 | 67150258 | intron variant | C/T | snv | 0.17 | 8 | ||
rs2266959 | 0.776 | 0.200 | 22 | 21568615 | intron variant | G/T | snv | 0.18 | 8 | ||
rs34920465 | 0.807 | 0.160 | 1 | 22373858 | intergenic variant | A/G | snv | 0.24 | 7 | ||
rs78534766 | 0.827 | 0.080 | 16 | 50301163 | missense variant | C/A | snv | 4.3E-03 | 3.6E-03 | 7 | |
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 7 | ||
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 7 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 7 | ||
rs11229555 | 0.827 | 0.120 | 11 | 58641214 | intron variant | G/T | snv | 0.21 | 7 | ||
rs1182188 | 0.827 | 0.120 | 7 | 2830351 | intron variant | T/C | snv | 0.26 | 7 | ||
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 7 | |
rs3024493 | 0.776 | 0.280 | 1 | 206770623 | intron variant | C/A;T | snv | 0.11 | 7 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
rs3197999 | 0.732 | 0.280 | 3 | 49684099 | missense variant | G/A | snv | 0.26 | 0.27 | 7 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 7 | ||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 6 | |||
rs1569328 | 0.827 | 0.120 | 14 | 75275048 | upstream gene variant | C/T | snv | 0.12 | 6 | ||
rs16967103 | 0.827 | 0.120 | 15 | 38606989 | intergenic variant | T/C | snv | 0.22 | 6 | ||
rs17085007 | 0.827 | 0.120 | 13 | 26957130 | regulatory region variant | T/C | snv | 0.16 | 6 | ||
rs2050392 | 0.827 | 0.120 | 10 | 30402574 | downstream gene variant | G/A | snv | 0.45 | 6 | ||
rs2143178 | 0.827 | 0.120 | 22 | 39264824 | intron variant | T/C | snv | 0.19 | 6 | ||
rs2538470 | 0.827 | 0.120 | 7 | 148523356 | intergenic variant | A/G | snv | 0.61 | 6 | ||
rs4243971 | 0.827 | 0.120 | 20 | 32261714 | intergenic variant | T/G | snv | 0.64 | 6 | ||
rs4703855 | 0.827 | 0.120 | 5 | 72398072 | regulatory region variant | C/T | snv | 0.24 | 6 | ||
rs559928 | 0.827 | 0.120 | 11 | 64382898 | intergenic variant | T/C | snv | 0.77 | 6 |