Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 25 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 | |
rs11174202 | 0.925 | 0.040 | 12 | 61858476 | intron variant | A/G | snv | 0.49 | 2 | ||
rs12504244 | 0.925 | 0.040 | 4 | 54619021 | intergenic variant | C/A;G;T | snv | 2 | |||
rs4633 | 0.695 | 0.400 | 22 | 19962712 | synonymous variant | C/T | snv | 0.46 | 0.45 | 2 | |
rs5030980 | 0.925 | 0.120 | 16 | 67483042 | missense variant | C/T | snv | 3.2E-02 | 2.9E-02 | 2 | |
rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 2 | |
rs75063949 | 0.925 | 0.040 | 6 | 25590813 | intron variant | C/G | snv | 0.14 | 2 | ||
rs929626 | 0.925 | 0.120 | 5 | 158883623 | intron variant | A/G | snv | 0.40 | 2 | ||
rs10747478 | 1.000 | 0.040 | 1 | 96435899 | intergenic variant | T/A;C;G | snv | 1 | |||
rs117957029 | 1.000 | 0.040 | 12 | 127200688 | intron variant | T/C | snv | 1.4E-02 | 1 | ||
rs1285957 | 1.000 | 0.040 | 7 | 141889478 | downstream gene variant | T/C | snv | 0.86 | 1 | ||
rs13100344 | 1.000 | 0.040 | 3 | 94886263 | intergenic variant | T/A | snv | 0.40 | 1 | ||
rs13125782 | 1.000 | 0.040 | 4 | 7426539 | intron variant | T/A;C;G | snv | 1 | |||
rs145241704 | 1.000 | 0.040 | 7 | 141805287 | upstream gene variant | T/G | snv | 7.4E-02 | 1 | ||
rs200312312 | 1.000 | 0.040 | 5 | 104666645 | intron variant | T/C | snv | 0.16 | 1 | ||
rs2008387 | 1.000 | 0.040 | 10 | 129650500 | intron variant | G/A | snv | 0.36 | 1 | ||
rs2287348 | 1.000 | 0.040 | 2 | 53812676 | intron variant | C/A;T | snv | 1 | |||
rs370838138 | 1.000 | 0.040 | 5 | 25081736 | intergenic variant | G/C | snv | 0.42 | 1 | ||
rs4622308 | 0.925 | 0.160 | 12 | 56075401 | upstream gene variant | C/T | snv | 1 | |||
rs4684677 | 0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 | 1 | |
rs533123 | 0.882 | 0.160 | 1 | 28814643 | intron variant | G/A;C | snv | 1 | |||
rs56156506 | 1.000 | 0.040 | X | 38140399 | intron variant | A/T | snv | 0.33 | 1 | ||
rs62090893 | 1.000 | 0.040 | 18 | 75338379 | intergenic variant | G/A | snv | 9.7E-02 | 1 | ||
rs6589488 | 1.000 | 0.040 | 11 | 115226236 | intron variant | A/T | snv | 0.90 | 1 |