Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs11721827
TLR3
0.851 0.200 4 186069983 intron variant A/C snv 0.12 4
rs17026425
IQCM
0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs1970764
PPP1R13L
0.851 0.120 19 45387615 intron variant T/C snv 0.27 4
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs2632159
LOC105375751 ; PCAT1
0.882 0.080 8 127021159 intron variant G/A;T snv 3
rs322351
DUSP1
0.925 0.160 5 172767870 intron variant C/T snv 0.37 3
rs10889675
IL23R
1.000 0.080 1 67256533 intron variant C/A snv 0.11 2
rs17268122
ABCC4
1.000 0.080 13 95192240 intron variant G/A;C;T snv 2
rs2073438
ALOX12 ; ALOX12-AS1
0.925 0.160 17 6996757 intron variant G/A snv 0.20 2
rs7542081
IL23R
1.000 0.080 1 67237570 intron variant C/A snv 0.56 2
rs10857561
MAPK8
1.000 0.080 10 48400595 intron variant G/A snv 0.29 1
rs11247735
SELENON
1.000 0.080 1 25804968 intron variant G/A;C snv 1
rs11718498
TXNRD3
1.000 0.080 3 126654076 intron variant G/A snv 0.36 1