Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs779745819
SLC26A4-AS1 ; SLC26A4
1.000 0.080 7 107663393 missense variant G/A snv 1.6E-05 2.8E-05 2
rs17154353
SLC26A4
0.925 0.080 7 107710182 missense variant G/A;T snv 3.7E-03; 8.0E-06 3
rs7528153
VAV3
0.925 0.080 1 107765105 missense variant T/A snv 0.58 0.64 4
rs281874674
COL4A5
0.827 0.280 X 108597479 missense variant G/C;T snv 8
rs104886142
COL4A5
0.790 0.280 X 108598793 missense variant G/A snv 8.7E-05 4.7E-05 10
rs11544331
C7orf50 ; GPER1
0.925 0.080 7 1091775 missense variant C/T snv 0.21 0.19 5
rs11879293
SMARCA4
0.882 0.120 19 10961934 intron variant G/A;C;T snv 4
rs1344469579
GSTM2 ; GSTM1
1 109688179 missense variant G/A snv 1
rs11807
GSTM5
1 109718120 3 prime UTR variant T/C snv 0.17 1
rs9899362 17 10977893 intergenic variant A/G;T snv 1
rs10491093 17 10978681 intergenic variant T/G snv 0.72 1
rs11658572 17 10979696 intergenic variant C/T snv 0.58 1
rs9913883 17 10980479 intergenic variant G/A snv 0.12 1
rs218966
PHF14
7 10982603 missense variant A/G snv 0.64 0.68 2
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs10033366
ENPEP
4 110409934 intron variant T/C snv 0.92 1
rs76425569
COL4A2
1.000 0.120 13 110449695 synonymous variant G/A snv 0.31 0.28 2
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs531003 9 110850339 intergenic variant G/C;T snv 1
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5