Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 5
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 5
rs13095226
COL8A1
0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 5
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs73036519
EXOC3L2 ; MARK4
0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs11884770
COL4A3 ; MFF-DT
0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs181705462
CYP21A2 ; STK19
0.851 0.040 6 31979250 intron variant G/C;T snv 4
rs187328863
KCNT2
0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs191281603
CFHR5
0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4