Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4418214 0.925 0.040 6 31423624 intron variant T/C snv 7.7E-02 5
rs4711268 1.000 6 31386727 upstream gene variant C/T snv 0.31 5
rs4711269 1.000 6 31387042 upstream gene variant C/T snv 0.32 5
rs554543329 1.000 6 30971106 intergenic variant A/G snv 5
rs6932730 0.925 6 31386405 upstream gene variant T/C snv 0.26 5
rs6933050 0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22 5
rs719654 0.925 0.120 6 32784362 intergenic variant G/A snv 0.21 5
rs7751505 1.000 6 31392478 downstream gene variant A/C snv 0.31 5
rs7751725 1.000 6 31392656 downstream gene variant A/G snv 0.31 5
rs9266409 0.925 0.200 6 31368791 intron variant T/C snv 0.22 5
rs9368649 0.925 0.040 6 30971106 intergenic variant A/G snv 0.10 5
rs9378200 0.925 0.120 6 31605150 intergenic variant T/C snv 5.4E-02 5
rs111182473 1.000 6 31385912 upstream gene variant G/A;T snv 4
rs11753208 1.000 6 31037655 downstream gene variant C/T snv 9.7E-02 4
rs12185555 1.000 2 226694601 regulatory region variant A/G snv 0.25 4
rs13198903 1.000 6 31376380 upstream gene variant C/T snv 6.3E-02 4
rs13202464 0.925 0.040 6 31376806 upstream gene variant A/G snv 6.3E-02 4
rs16948255 1.000 16 74847922 downstream gene variant C/T snv 3.9E-02 4
rs17207190 1.000 6 31601743 intergenic variant G/A;T snv 2.8E-02 4
rs17324272 1.000 X 133003128 intergenic variant T/C snv 3.2E-03 4
rs2394894 1.000 6 31239143 intergenic variant T/C snv 0.21 4
rs2394895 1.000 6 31239202 intergenic variant T/C snv 0.21 4
rs2394944 1.000 6 31252673 regulatory region variant C/T snv 0.21 4
rs2507976 1.000 6 31384110 upstream gene variant C/A;T snv 4
rs2515919 1.000 6 31596390 upstream gene variant A/G snv 0.31 4