Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17216707 | 20 | 54115823 | intergenic variant | T/C | snv | 0.17 | 6 | ||||
rs6127099 | 20 | 54114863 | intergenic variant | A/T | snv | 0.28 | 5 | ||||
rs10485165 | 6 | 88403098 | intron variant | C/G;T | snv | 3 | |||||
rs2302190 | 17 | 58507147 | missense variant | T/A;C | snv | 0.24 | 3 | ||||
rs78862524 | 4 | 72305473 | intron variant | C/A | snv | 3.9E-02 | 3 | ||||
rs1007392 | 11 | 14753045 | intron variant | A/G | snv | 0.35 | 2 | ||||
rs10745742 | 12 | 95964751 | intron variant | C/T | snv | 0.48 | 2 | ||||
rs11023332 | 11 | 14762564 | intron variant | G/C | snv | 0.35 | 2 | ||||
rs11586313 | 1 | 152917994 | TF binding site variant | G/A;C | snv | 0.51 | 2 | ||||
rs116970203 | 11 | 14855172 | intron variant | G/A | snv | 2.2E-02 | 2 | ||||
rs117300835 | 11 | 15097429 | intergenic variant | G/A | snv | 7.6E-03 | 2 | ||||
rs117865811 | 11 | 14180763 | intron variant | A/G | snv | 6.3E-03 | 2 | ||||
rs117913124 | 11 | 14879385 | synonymous variant | G/A | snv | 1.7E-02 | 1.6E-02 | 2 | |||
rs12287212 | 11 | 14428315 | intergenic variant | C/A | snv | 0.31 | 2 | ||||
rs12868495 | 13 | 34067425 | intergenic variant | G/A | snv | 2.3E-02 | 2 | ||||
rs13107347 | 4 | 72109031 | intron variant | T/C | snv | 0.32 | 2 | ||||
rs138485827 | 4 | 72166226 | intergenic variant | C/T | snv | 5.0E-02 | 2 | ||||
rs1410656 | 13 | 46968386 | intergenic variant | T/C | snv | 0.97 | 2 | ||||
rs148189294 | 4 | 71575200 | downstream gene variant | G/A | snv | 2.6E-02 | 2 | ||||
rs1526692 | 4 | 71713007 | intergenic variant | A/G | snv | 0.41 | 2 | ||||
rs156299 | 7 | 24185113 | intergenic variant | T/G | snv | 0.53 | 2 | ||||
rs1607741 | 4 | 71853316 | intergenic variant | G/C | snv | 0.65 | 2 | ||||
rs17767445 | 4 | 71879550 | intergenic variant | G/A | snv | 0.20 | 2 | ||||
rs182244780 | 11 | 14363985 | intron variant | G/A | snv | 6.0E-03 | 2 | ||||
rs185378533 | 11 | 71422087 | intron variant | A/G | snv | 0.68 | 2 |