Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17596143 11 55910869 downstream gene variant T/A snv 5.7E-02 1
rs17597169 11 55921634 intergenic variant T/C snv 5.8E-02 1
rs17597302 11 55922387 intergenic variant C/T snv 5.8E-02 1
rs17598045 11 55940815 upstream gene variant G/A;T snv 1
rs17598094 11 55941339 upstream gene variant T/C snv 6.0E-02 1
rs17599471 11 55959133 upstream gene variant G/A snv 6.1E-02 1
rs17602278 11 56081639 upstream gene variant T/C snv 6.0E-02 1
rs17603373 11 56118743 upstream gene variant T/C snv 5.8E-02 1
rs17610514 11 56128322 downstream gene variant A/G snv 6.0E-02 1
rs1876924 11 56580160 upstream gene variant G/A snv 5.9E-02 1
rs1957563 5 158047582 intergenic variant C/T snv 0.25 1
rs2145067 6 94547045 intergenic variant C/T snv 0.16 1
rs2702888 8 6907510 intergenic variant G/A;C;T snv 1
rs2969070 7 2472910 downstream gene variant G/A;C snv 1
rs35444 12 115114632 intergenic variant A/G snv 0.38 1
rs4141856 19 50865248 intron variant C/T snv 0.61 1
rs4638749 2 108267586 downstream gene variant G/A snv 0.26 1
rs4685307 3 16123911 regulatory region variant G/A;T snv 1
rs4842666 12 89547772 non coding transcript exon variant T/C snv 0.16 1
rs4977950 9 24732484 intergenic variant G/C;T snv 1
rs6763470 3 55390915 intergenic variant T/A;G snv 1
rs6892243 5 104843088 intron variant G/A snv 9.0E-02 1
rs7088591 10 57964643 regulatory region variant A/T snv 9.3E-02 1
rs7108801 11 56309124 intergenic variant C/T snv 5.9E-02 1
rs7110667 11 34006534 regulatory region variant A/T snv 0.22 1