Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10456943 6 121556819 regulatory region variant A/C snv 0.11 1
rs10460436 2 231950631 intergenic variant G/A snv 5.7E-02 1
rs10463076 5 160177301 intergenic variant G/A snv 0.16 1
rs10472828 5 32888712 non coding transcript exon variant C/T snv 0.40 1
rs10479944 7 15074211 intergenic variant T/A snv 0.13 1
rs10514714 3 46594334 intron variant G/T snv 5.9E-02 1
rs10516446 4 99629967 upstream gene variant T/A snv 0.19 1
rs10517245 4 52163519 intergenic variant G/A snv 0.15 1
rs10519170 15 48393978 regulatory region variant A/G snv 0.18 1
rs1052483 2 219069626 non coding transcript exon variant G/T snv 0.13 1
rs10526240 11 58004066 upstream gene variant T/A;G snv 1
rs10746837 9 88258738 regulatory region variant G/A snv 0.49 1
rs10747784 12 57857579 intergenic variant G/A;C;T snv 1
rs10748128 12 69433878 intergenic variant G/T snv 0.42 1
rs10756851 9 16991334 intron variant G/A snv 0.50 1
rs10773100 12 124695033 TF binding site variant C/G;T snv 1
rs10779122 12 84661783 regulatory region variant T/C snv 0.36 1
rs10781573 10 132420104 intron variant C/A;T snv 0.69 1
rs10784445 12 65272610 intergenic variant A/G;T snv 1
rs10795075 10 3773988 downstream gene variant C/T snv 0.35 1
rs10798580 1 177895419 intron variant G/A snv 0.36 1
rs10799445 1 227724182 upstream gene variant A/C snv 0.27 1
rs10811888 9 23325086 intron variant T/C snv 0.52 1
rs10826579 10 29202607 regulatory region variant G/A;T snv 1
rs10847415 12 122659746 regulatory region variant T/A;C snv 1