Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 7
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 6
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 5
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5