Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7