Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs2066363 0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6689858 0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs17849502 0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs864537 0.925 0.200 1 167442147 intron variant A/G snv 0.29 3
rs12068671 0.925 0.160 1 172711891 intergenic variant T/C snv 0.23 2
rs12734338 0.925 0.120 1 202500595 intron variant T/C snv 2
rs1359062 0.925 0.160 1 192572342 intron variant C/A;G;T snv 2
rs3748816 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 2
rs4073285 0.925 0.200 1 2608357 intron variant C/T snv 0.40 2
rs6696533 0.925 0.200 1 198764438 intergenic variant T/C snv 0.28 2
rs10800746 1.000 0.080 1 200912264 intron variant C/T snv 0.32 1
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 1
rs12142280 1.000 0.080 1 172895512 intron variant T/A snv 0.21 1
rs12727642 1.000 0.080 1 7986612 upstream gene variant C/A snv 0.12 1
rs2157453 1.000 0.080 1 172894808 intron variant G/A snv 0.31 1
rs2816316 0.882 0.200 1 192567683 intron variant C/A snv 0.79 1
rs296547 0.882 0.200 1 200923009 intron variant T/C snv 0.53 1
rs4445406 1.000 0.080 1 2607961 intron variant T/C snv 0.41 1
rs59655222 1.000 0.080 1 200906769 intron variant T/C snv 0.22 1