Disease: Atrial Fibrillation
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 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
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 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
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22