Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7694379 1.000 4 87265357 intron variant G/A snv 0.40 3
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs10510050 10 118867050 intron variant A/G snv 0.52 1
rs9574547 13 80057282 intron variant C/A snv 0.17 1
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs766715154
ABCC4
13 95206759 missense variant T/C;G snv 4.0E-06 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1554785242
ADAMTS13
0.882 0.160 9 133426240 missense variant G/T snv 8
rs1554791280
ADAMTS13
0.882 0.160 9 133442718 missense variant T/C snv 8
rs1554800065
ANKRD26
1.000 0.120 10 27100445 5 prime UTR variant G/C snv 2
rs863223318
ANKRD26
1.000 0.120 10 27100460 5 prime UTR variant C/T snv 2
rs28362731
AQP1
7 30922175 missense variant G/A snv 3.1E-02 2.6E-02 2
rs11789898
BRD3
9 134060541 intron variant G/T snv 0.14 3
rs1537514
C1orf167 ; MTHFR
0.882 0.120 1 11788011 missense variant G/C snv 0.10 0.10 4
rs2290280
CCNH ; LOC105379066
5 87412904 5 prime UTR variant C/A;T snv 1
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs1553196096
CDC42
1 22086463 missense variant G/A snv 5
rs555607708
CHEK2
0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs121908065
CHRNE ; GP1BA
0.851 0.080 17 4933119 missense variant C/T snv 5
rs757788894
CLCN7
0.882 0.120 16 1449081 missense variant C/T snv 4.0E-06 6
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs121918552
CYCS
1.000 0.040 7 25123996 missense variant C/T snv 2
rs4986910
CYP3A4
0.925 0.080 7 99760901 missense variant A/G snv 5.2E-03 5.1E-03 3