Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1040552 20 33861523 regulatory region variant A/G snv 0.19 2
rs12465955 2 127249498 non coding transcript exon variant A/G;T snv 2
rs12625191 20 35623371 downstream gene variant C/G snv 6.7E-02 2
rs13037376 20 35297352 upstream gene variant T/C snv 0.35 2
rs13038810 20 36282301 intergenic variant A/C;G snv 2
rs13041173 20 33955008 intergenic variant A/G snv 0.25 2
rs1566822 2 127229815 intergenic variant A/G snv 0.40 2
rs1604817 2 127242345 upstream gene variant C/T snv 0.61 2
rs17302686 20 34322499 TF binding site variant G/A snv 4.0E-02 2
rs17332951 20 34176377 regulatory region variant T/C snv 3.6E-02 2
rs2092477 20 33896623 regulatory region variant T/A;C snv 2
rs2174270 2 127248502 non coding transcript exon variant C/G;T snv 2
rs224320 20 35422754 intergenic variant G/A snv 0.88 2
rs2425207 20 36271121 downstream gene variant G/A snv 7.9E-02 2
rs2425215 20 36282083 intergenic variant T/G snv 0.12 2
rs2425219 20 36286427 intergenic variant C/A;T snv 2
rs3761135 20 35744478 upstream gene variant C/T snv 7.0E-02 2
rs4324393 20 33949027 intergenic variant G/A;C snv 2
rs4510165 2 127178708 intergenic variant C/T snv 0.10 2
rs4536600 2 127244996 upstream gene variant G/A snv 0.59 2
rs4662713 2 127236527 intergenic variant C/A;T snv 2
rs4662717 2 127255928 downstream gene variant C/T snv 0.47 2
rs4663109 2 127164716 intergenic variant A/G snv 0.78 2
rs4911134 20 33864409 intergenic variant C/T snv 0.18 2
rs4911369 20 33864370 intergenic variant T/C snv 0.20 2