Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10209110
AFF3
1.000 0.120 2 100056230 intron variant C/T snv 0.47 1
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs11123811
AFF3
1.000 0.120 2 100143710 intron variant T/C snv 0.55 1
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs9653442
LINC01104
1.000 0.120 2 100208905 intron variant C/T snv 0.46 2
rs34619498
EMCN
1.000 0.120 4 100505575 intron variant T/C snv 2.3E-02 1
rs10275421
LNCPRESS1
1.000 0.120 7 101299780 non coding transcript exon variant G/A snv 7.2E-02 1
rs678347 1.000 0.120 8 101451374 intron variant G/A;C snv 1
rs646514 1.000 0.120 8 101453833 upstream gene variant C/G;T snv 1
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs948138
LOC101928477
1.000 0.120 11 102630934 downstream gene variant G/A snv 0.59 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 1
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 6
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs39984
MACIR
1.000 0.120 5 103261591 intron variant G/T snv 0.30 1
rs2561477
MACIR
1.000 0.120 5 103273223 intron variant G/A snv 0.24 1
rs7258015
ICAM3
0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs4918037
SH3PXD2A
1.000 0.120 10 103653282 intron variant A/G snv 0.88 1
rs4264325
TMEM179
1.000 0.120 14 104513149 intron variant T/C snv 0.97 1