Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6778062 3 133548309 upstream gene variant G/C snv 0.66 1
rs2677485 2 155678644 intergenic variant T/A;C snv 1
rs12108602 4 114719413 upstream gene variant A/G snv 0.18 1
rs1444600 3 133569662 upstream gene variant C/T snv 0.57 1
rs855350 1 63661333 downstream gene variant C/T snv 0.43 1
rs872134 3 133546688 upstream gene variant G/T snv 0.57 1
rs10249276 7 118938630 intergenic variant A/G;T snv 1
rs1995364 1.000 0.080 5 10903669 intergenic variant A/G snv 0.62 1
rs17616845 1.000 0.080 7 12741918 intron variant T/C snv 0.15 1
rs6777876 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 1
rs6701037 1.000 0.080 1 175150943 downstream gene variant A/C;T snv 1
rs4384980 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 1
rs994029 1.000 0.080 9 86760399 downstream gene variant C/T snv 0.71 1
rs4610908 1.000 0.080 X 35166418 intergenic variant G/A snv 0.24 1
rs7777391 1.000 0.080 7 117981823 intergenic variant A/G snv 0.60 1
rs7607774 1.000 0.080 2 236520511 intergenic variant G/A snv 7.4E-02 1
rs6425323 1.000 0.080 1 175155900 downstream gene variant C/T snv 0.39 1
rs17028719 1.000 0.080 1 5734948 intergenic variant A/G snv 4.8E-02 1
rs9847462 1.000 0.080 3 164840807 intergenic variant A/G snv 0.14 1
rs9982439 1.000 0.040 21 42329090 regulatory region variant T/C snv 3.1E-02 1
rs9479482 1.000 0.040 6 150036876 downstream gene variant T/C snv 0.36 1
rs7682241 1.000 0.040 4 122602720 regulatory region variant G/T snv 0.30 1
rs3099624 1.000 0.040 1 11436937 intergenic variant C/T snv 0.34 1
rs11224294 0.925 0.080 11 100578431 regulatory region variant T/C snv 9.9E-02 1
rs2666138 1.000 0.040 2 36104014 intergenic variant G/A;T snv 1