Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16