Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10749071 10 111334279 intergenic variant A/G;T snv 1
rs11728925 4 41711648 intergenic variant C/A;T snv 1
rs11913168 22 30210575 upstream gene variant G/A snv 0.12 1
rs1792624 11 94188644 non coding transcript exon variant G/A snv 0.31 1
rs4809944 20 53885423 TF binding site variant A/C;G snv 1
rs4897668 8 134018372 intergenic variant A/G snv 0.46 1
rs7830326
ADAM32
8 39210657 intron variant A/G snv 0.46 1
rs13070790
ALCAM
3 105417143 intron variant C/G;T snv 1
rs4823231
ATXN10
22 45692239 intron variant T/A;C snv 1
rs121909588
C5
1.000 0.080 9 120962749 stop gained G/A snv 7.6E-05 1.7E-04 2
rs112959008
C5
9 121030401 missense variant C/G;T snv 3.2E-04 1
rs121964921
C7
1.000 0.080 5 40955428 missense variant G/A;C;T snv 1.6E-05; 1.3E-04; 5.3E-05 2
rs2244614
CES1
16 55810705 intron variant G/A snv 0.52 0.50 1
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs426736
CFHR3
1.000 0.040 1 196791287 intron variant A/G snv 0.28 2
rs2420864
CNTNAP5
2 124459809 intron variant T/A;C snv 1
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs4556879
FBXO15
18 74138268 intron variant C/T snv 4.3E-02 1
rs655683
GRM5
11 88943686 intron variant G/T snv 0.27 1
rs1299491
IL4I1 ; NUP62
19 49916142 intron variant A/C snv 0.70 1
rs370867162
MBL2
10 52768257 missense variant G/A;T snv 6.4E-05 8.4E-05 1
rs4976846
MYO16 ; MYO16-AS1
13 109168863 intron variant T/C snv 0.29 1
rs4972431
OLA1
2 174134460 intron variant C/T snv 0.53 1
rs10838427
PRDM11
11 45160131 intron variant C/T snv 0.30 1
rs397728201
SFTPA1
0.925 0.160 10 79614033 stop gained C/A;T snv 3.6E-05; 4.0E-06 4