Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10096633 | 1.000 | 0.040 | 8 | 19973410 | regulatory region variant | C/T | snv | 0.22 | 7 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 2 | |
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 10 | ||
rs10503669 | 0.925 | 0.080 | 8 | 19990179 | intergenic variant | C/A | snv | 8.4E-02 | 7 | ||
rs10738760 | 0.807 | 0.320 | 9 | 2691186 | regulatory region variant | A/G | snv | 0.56 | 1 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 4 | ||
rs10790162 | 0.882 | 0.160 | 11 | 116768388 | intron variant | A/G;T | snv | 0.93 | 3 | ||
rs10830956 | 1.000 | 0.040 | 11 | 92947847 | intergenic variant | C/T | snv | 0.33 | 1 | ||
rs10830962 | 0.851 | 0.160 | 11 | 92965261 | upstream gene variant | C/A;G;T | snv | 4 | |||
rs10838681 | 1.000 | 0.040 | 11 | 47253513 | intron variant | G/A | snv | 0.34 | 1 | ||
rs10849915 | 0.925 | 0.080 | 12 | 110895818 | intron variant | T/C | snv | 0.39 | 2 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 5 | ||
rs11063069 | 0.925 | 0.080 | 12 | 4265207 | intron variant | A/G | snv | 0.20 | 1 | ||
rs11065756 | 0.925 | 0.080 | 12 | 110900990 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs11066001 | 0.763 | 0.360 | 12 | 111681367 | intron variant | T/C | snv | 5.8E-03 | 2 | ||
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 8 | ||
rs11216126 | 1.000 | 0.040 | 11 | 116746524 | downstream gene variant | A/C | snv | 0.11 | 2 | ||
rs1127065 | 1.000 | 0.040 | 7 | 44220272 | synonymous variant | C/G;T | snv | 1.7E-02; 0.41 | 1 | ||
rs11600380 | 1.000 | 0.040 | 11 | 116799466 | intergenic variant | T/C | snv | 6.6E-02 | 2 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 4 | ||
rs11722228 | 0.851 | 0.160 | 4 | 9914117 | intron variant | C/T | snv | 0.32 | 4 | ||
rs11773845 | 0.925 | 0.120 | 7 | 116551247 | intron variant | C/A | snv | 0.53 | 1 | ||
rs11820589 | 1.000 | 0.040 | 11 | 116763146 | missense variant | G/A | snv | 7.8E-02 | 0.10 | 5 | |
rs11868035 | 0.763 | 0.200 | 17 | 17811787 | splice region variant | G/A | snv | 0.45 | 0.33 | 1 |