Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs2252865 0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs10503253 0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs12325410 0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs12966547 0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs1715 0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs17662626 0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2021722 0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800 0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs2799573 0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs3132581 0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs548181 0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs7004633 0.851 0.040 8 88748082 intron variant A/G snv 0.28 5