Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795550
ITIH5
1.000 0.040 10 7562392 3 prime UTR variant T/C;G snv 0.88 1
rs9350591 0.925 0.040 6 75531811 intergenic variant C/A;T snv 0.12 2
rs11688000
TACR1
1.000 0.040 2 75066030 intron variant A/G snv 0.34 1
rs35206230 1.000 0.040 15 74805439 downstream gene variant C/T snv 0.43 1
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1042667
SOX9-AS1 ; SOX9
1.000 0.040 17 72124410 3 prime UTR variant A/C snv 0.41 0.36 3
rs12601701
SOX9-AS1 ; LOC107987249 ; SOX9
1.000 0.040 17 72119217 intron variant G/A snv 0.35 1
rs4747096
ADAMTS14
0.925 0.040 10 70758253 missense variant A/G;T snv 0.19 0.19 2
rs3771501
TGFA
0.925 0.040 2 70490521 intron variant A/G snv 0.60 2
rs2862851
TGFA
1.000 0.040 2 70485670 intron variant T/C snv 0.58 1
rs317630
CPSF6
1.000 0.040 12 69244067 intron variant T/C snv 0.76 1
rs7164503
ANP32A
0.925 0.040 15 68789051 intron variant T/C snv 0.27 2
rs3743342
SMAD3
1.000 0.040 15 67193329 3 prime UTR variant C/T snv 0.20 1
rs12595334
SMAD3
1.000 0.040 15 67192818 3 prime UTR variant C/T snv 0.19 1
rs8031440
SMAD3
1.000 0.040 15 67191641 3 prime UTR variant G/A snv 0.19 1
rs2289263
SMAD3
0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs12102171
SMAD3
1.000 0.040 15 67132695 intron variant C/T snv 0.22 1
rs6494629
SMAD3
0.925 0.120 15 67081773 intron variant C/T snv 0.52 2
rs12901499
SMAD3
0.882 0.040 15 67078107 intron variant G/A snv 0.45 3
rs12901071
SMAD3
0.882 0.160 15 67078051 intron variant A/G snv 0.25 3
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2073711
CILP
0.807 0.160 15 65201874 missense variant A/G snv 0.56 0.61 7
rs1256049
ESR2
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9