Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150803770 3 49432529 upstream gene variant -/GTTTATTT;TTTTATTT;TTTTATTTATTT;TTTTATTTATTTATTT;TTTTATTTATTTATTTATTT delins 2
rs1548770 14 74219855 intergenic variant C/T snv 0.88 2
rs17564336 1 151376698 upstream gene variant G/T snv 0.24 2
rs17616464 14 103373661 downstream gene variant C/G snv 6.5E-02 2
rs181042996 16 67204767 upstream gene variant G/A;T snv 2
rs1831149 9 86729522 intergenic variant A/G snv 0.49 2
rs192277252 7 32913216 downstream gene variant C/A snv 2.0E-02 2
rs193104780 6 108775380 intergenic variant G/A snv 4.7E-03 2
rs1962929 18 46467224 downstream gene variant G/A snv 0.24 2
rs2036321 5 123502807 intergenic variant C/T snv 0.22 2
rs2115563 6 53357184 downstream gene variant A/C;G snv 2
rs2178658 7 87492706 intergenic variant G/C;T snv 0.24 2
rs2254594 7 17773990 intergenic variant G/A;T snv 2
rs2412771 4 56895251 intergenic variant T/C snv 0.36 2
rs2806029 14 72964752 upstream gene variant A/G;T snv 2
rs28444102 16 169498 upstream gene variant G/A;T snv 2
rs292168 5 36807087 intergenic variant A/G;T snv 2
rs2954027 8 125473052 intron variant T/A snv 0.48 2
rs2965199 19 19364279 intergenic variant G/A;C snv 0.57 2
rs2974366 8 42576625 intergenic variant C/A;G;T snv 2
rs3130901 6 31451288 intron variant A/T snv 0.23 2
rs322353 5 172765865 intron variant T/C snv 0.48 2
rs34255979 19 45881572 downstream gene variant C/T snv 0.11 2
rs34578041 7 36130799 intergenic variant T/A;C snv 2
rs34595852 9 86263457 upstream gene variant -/CT delins 0.75 2