Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10444602 12 131708291 upstream gene variant T/G snv 0.51 1
rs11659639 18 60500379 intron variant T/G snv 1.1E-02 1
rs1173766 5 32804422 intergenic variant T/C snv 0.57 1
rs11816631 10 97802815 intergenic variant A/G snv 8.8E-02 1
rs12067906 1 192462868 intron variant T/C snv 0.12 1
rs12098903 11 55899037 downstream gene variant A/T snv 5.7E-02 1
rs12098904 11 55899077 downstream gene variant A/T snv 5.7E-02 1
rs12098941 11 55898967 downstream gene variant T/A;G snv 1
rs13002573 2 164058698 intron variant A/G snv 0.20 1
rs13149993 4 80237391 regulatory region variant G/A;C snv 1
rs13209747 6 126794309 intron variant C/G;T snv 0.36 1
rs1384089 11 56081540 upstream gene variant G/C snv 6.0E-02 1
rs1446468 2 164106976 intron variant T/C snv 0.40 1
rs1492840 4 45764988 intergenic variant A/C;G;T snv 1
rs16833934 3 164019462 intergenic variant A/G snv 0.34 1
rs16849225 2 164050310 intron variant C/T snv 0.19 1
rs16877320 6 15922795 TF binding site variant T/A;C snv 1
rs17428471 7 27298248 intergenic variant G/T snv 9.4E-02 1
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 1
rs17510438 11 55902839 downstream gene variant G/A snv 5.7E-02 1
rs17511107 11 55908549 upstream gene variant T/C snv 5.7E-02 1
rs17512592 11 55922766 intergenic variant A/G snv 5.8E-02 1
rs17530228 11 56081680 upstream gene variant A/G snv 6.0E-02 1
rs17531933 11 56128173 downstream gene variant T/C;G snv 1
rs17531954 11 56128255 downstream gene variant T/C snv 6.0E-02 1