Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10490924
ARMS2 ; LOC105378525
0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs10507047
FGD6
0.925 0.040 12 95210514 missense variant T/C snv 0.12 0.11 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1064039
CST3
0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1136287
SERPINF1
0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 5
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 5
rs11775442
ANGPT2 ; MCPH1
0.925 0.040 8 6538837 intron variant A/G snv 0.20 2
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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs12661281
SLC44A4 ; CYP21A2
0.882 0.040 6 31874821 missense variant T/A snv 0.15 0.11 3
rs13095226
COL8A1
0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5