Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs44707
ADAM33
0.925 0.080 20 3670579 non coding transcript exon variant G/C;T snv 2
rs4914
TMCO6 ; CD14
0.925 0.160 5 140631883 synonymous variant C/A;G snv 4.8E-05; 9.3E-02 2
rs5875060
SCGN
1.000 0.080 6 25701740 3 prime UTR variant T/-;TT;TTT delins 2
rs5953283
PPP1R3F
0.925 0.080 X 49283326 intron variant A/G;T snv 2
rs6503525
LRRC3C
0.925 0.080 17 39938921 intron variant G/A;C snv 2
rs6755248
AP1S3
0.925 0.080 2 223799333 intron variant C/G;T snv 2
rs678881
ADAM33
0.925 0.080 20 3669156 intron variant G/A;C snv 2
rs74180212 0.925 0.080 2 102181785 intron variant T/C;G snv 2
rs748245223
IL4R
0.925 0.080 16 27363275 synonymous variant C/T snv 4.1E-06 2
rs757568489
IL4R
0.925 0.080 16 27362545 missense variant G/A snv 4.0E-06 2
rs766736182
IL7
0.925 0.080 8 78733724 missense variant T/C snv 4.2E-06 2
rs766793834
TSPAN31
0.925 0.080 12 57747080 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs7705042
NDFIP1
0.925 0.080 5 142112854 intron variant C/A;T snv 2
rs8065126
LRRC3C
1.000 0.080 17 39942782 intron variant T/A;C snv 2
rs10175070
CCL20
1.000 0.080 2 227805859 5 prime UTR variant G/A;C snv 1
rs1220579705
IL4
1.000 0.080 5 132674079 missense variant C/T snv 1
rs1530976
SLC4A4
1.000 0.080 4 71527674 intron variant G/A;C snv 1
rs16925517
LINC01505
1.000 0.080 9 106484720 intron variant G/A;C snv 1
rs2289447
ATPAF1
1.000 0.080 1 46652496 non coding transcript exon variant C/G;T snv 1
rs2378383 1.000 0.080 9 79424447 intergenic variant A/C;G;T snv 1
rs2928442
LOC105378313
1.000 0.080 10 57386706 intergenic variant T/A;C snv 1
rs3814399
BOC
1.000 0.080 3 113272645 synonymous variant C/A;T snv 4.7E-04; 2.1E-02 1
rs439399
PDZD2
1.000 0.080 5 31696629 intron variant G/A;C;T snv 1
rs71421264
TRAF3
1.000 0.080 14 102777733 intron variant C/A;G;T snv 1