Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2007044 0.882 0.040 12 2235794 intron variant A/G snv 0.50 4
rs2054399 0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs4129585 1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs4356203 0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs4537545 0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs4870888 0.882 0.040 8 124096736 intron variant T/C snv 0.39 4
rs4925114 0.925 0.080 17 17807956 intron variant A/G snv 0.53 4
rs62173322 0.882 0.040 2 169754519 intron variant A/G snv 0.32 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6704768 1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs7219021 0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs7599488 0.925 0.120 2 60491212 intron variant C/T snv 0.42 4
rs76371172 0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs7872515 0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs8054556 0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs9268856 0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9272219 0.925 0.160 6 32634492 intron variant G/T snv 0.29 4
rs9467626 0.882 0.160 6 25873518 intron variant C/A snv 7.3E-02 4
rs951266 0.882 0.080 15 78586199 intron variant G/A snv 0.26 4
rs9577511 0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs10074991 0.851 0.120 5 40790449 intron variant G/A snv 0.31 3
rs10752262 1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs10774037 0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs11055980 1.000 0.040 12 14458588 intron variant C/T snv 0.40 3
rs11125080 0.882 0.040 2 46505266 intron variant G/A;C snv 3