Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 1
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 1
rs10438303 15 43724219 downstream gene variant T/C snv 0.16 1
rs10466588 11 116739533 regulatory region variant A/G snv 0.17 1
rs10474433 5 75321018 intron variant T/C snv 0.36 1
rs10475588 5 173227744 upstream gene variant T/C snv 2.1E-02 1
rs10495712 2 20973240 intergenic variant A/G snv 0.77 1
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 1
rs12326039 17 73155324 intergenic variant G/T snv 1.9E-02 1
rs12448528 16 56951643 TF binding site variant A/G snv 0.82 1
rs12678799 8 125458589 intergenic variant C/T snv 0.20 1
rs12679189 8 125461323 intergenic variant T/C snv 0.21 1
rs12755606 1 159700546 downstream gene variant C/G snv 0.24 1
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 1
rs1429974 2 21077898 intergenic variant C/A;T snv 1
rs1551894 5 75274706 intergenic variant G/A snv 0.20 1
rs1569209 8 19972659 regulatory region variant T/G snv 6.0E-02 1
rs17163738 7 142809818 downstream gene variant A/G snv 7.3E-02 1
rs17216525 19 19551411 downstream gene variant C/T snv 6.3E-02 1
rs17703271 17 27244140 upstream gene variant T/A;C snv 1
rs17730649 8 125453063 regulatory region variant C/A snv 0.53 1
rs1809986 11 48965987 downstream gene variant C/A;G snv 1
rs1871045 19 44823511 downstream gene variant C/T snv 0.39 1
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 1
rs2335418 5 75307654 intergenic variant G/A;C snv 1