Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 4
rs1490384 6 126530014 intron variant C/G;T snv 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 4
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs157595 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 3
rs1688043
HPN-AS1 ; HPN
19 35062437 intron variant C/G;T snv 3
rs340025
RORA ; RORA-AS1
15 60616108 intron variant T/A;C snv 3
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4910742
HBG2 ; HBE1
11 5285279 intron variant G/A;T snv 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 2
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs12072644 1 159245497 intergenic variant C/A;T snv 2
rs12427353
HNF1A
1.000 0.080 12 120989098 intron variant G/A;C;T snv 2
rs2251468
HNF1A-AS1
12 120967323 intron variant C/A;G;T snv 2