Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
rs13211318 0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11 5
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 5
rs17475879 0.925 0.040 6 30396731 regulatory region variant C/T snv 5.6E-02 5
rs2219893 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 5
rs2428486 0.925 0.120 6 31386327 upstream gene variant T/C snv 0.42 5
rs2517459 0.882 0.160 6 30929245 downstream gene variant T/C snv 0.74 5
rs2523554 0.925 0.080 6 31364052 upstream gene variant C/T snv 0.70 5
rs2621373 0.925 0.120 6 32797353 TF binding site variant T/A;C;G snv 5
rs2844477 0.925 0.120 6 31610995 upstream gene variant T/A;C snv 0.29 5
rs2844529 0.925 0.120 6 31385816 upstream gene variant G/A;T snv 5
rs3130424 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 5
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5