Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 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
rs13095226
COL8A1
0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5
rs1713985
REST
0.882 0.040 4 56920284 intron variant G/T snv 0.92 4
rs3750847
LOC105378525 ; ARMS2
0.882 0.040 10 122455905 intron variant C/T snv 0.23 4
rs429608
CYP21A2 ; SKIV2L
0.851 0.160 6 31962685 intron variant G/A snv 0.14 0.16 4
rs9621532
SYN3
0.851 0.040 22 32688525 intron variant A/C snv 5.8E-02 4
rs2511989
SERPING1
0.882 0.160 11 57610852 intron variant C/T snv 0.39 3
rs493258
ALDH1A2
0.925 0.040 15 58395681 intron variant T/C snv 0.50 3
rs547154
CYP21A2 ; C2 ; C2-AS1
0.882 0.160 6 31943161 intron variant G/T snv 0.12 3
rs6982567
C8orf37-AS1
0.882 0.040 8 95738053 intron variant C/T snv 0.24 3
rs11775442
ANGPT2 ; MCPH1
0.925 0.040 8 6538837 intron variant A/G snv 0.20 2
rs13269021
ANGPT2 ; MCPH1
0.925 0.040 8 6539242 intron variant G/A;T snv 2
rs225396
ABCG1
0.925 0.040 21 42267244 intron variant C/T snv 0.45 2
rs3173800
CD36
0.925 0.040 7 80660605 intron variant A/T snv 0.29 2
rs344555
C3
0.925 0.040 19 6679349 intron variant T/C snv 0.80 2
rs4455855
MCPH1 ; ANGPT2
0.925 0.040 8 6539909 intron variant A/T snv 0.57 2
rs868005
ELN
1.000 7 74030784 intron variant T/C snv 0.30 1
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10