Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11022114 11 12017327 regulatory region variant G/A snv 0.24 1
rs11079936 17 50830473 upstream gene variant T/C snv 0.56 1
rs11086556 20 38341570 upstream gene variant A/G snv 5.9E-02 1
rs11103602 9 134963026 regulatory region variant G/A snv 0.25 1
rs11103604 9 134965600 regulatory region variant G/A;T snv 1
rs111344982 6 32505811 intergenic variant T/A snv 1
rs111379368 1 67269677 upstream gene variant T/G snv 5.3E-02 1
rs11155591 6 148743850 upstream gene variant C/T snv 0.22 1
rs111577916 11 126201454 downstream gene variant G/A;T snv 1
rs11177623 12 40653549 intergenic variant T/C snv 0.29 1
rs112206797 14 105798591 intergenic variant A/G snv 7.0E-02 1
rs112226238 14 106074585 intergenic variant G/A snv 0.64 1
rs112255027 7 130231035 intergenic variant C/T snv 0.15 1
rs11229075 11 57623550 intergenic variant A/C snv 0.21 1
rs11229080 11 57632038 intergenic variant T/C snv 0.26 1
rs112702477 14 105563572 regulatory region variant T/G snv 2.8E-04 1
rs112782083 4 176834019 intergenic variant G/A;C snv 1.1E-02 1
rs11291564 1 160483182 downstream gene variant TT/-;T;TTT;TTTTTTTT delins 0.80 1
rs113265260 6 31422584 intron variant -/CA;CACA delins 1
rs113358888 14 106464462 upstream gene variant -/A delins 1
rs113534515 6 32493021 intergenic variant G/C;T snv 1
rs1138888 19 43191870 downstream gene variant T/A snv 0.69 1
rs114029601 6 31361252 upstream gene variant C/T snv 2.7E-02 1
rs114253244 6 37712127 regulatory region variant G/A snv 3.5E-02 1
rs114518757 19 48548356 non coding transcript exon variant T/C snv 4.7E-02 1