Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 9
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 7
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 6