Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs7775
FRZB
0.732 0.240 2 182834857 missense variant G/A;C;T snv 8.0E-05; 8.0E-02; 5.6E-05 14
rs1800668
GPX1
0.882 0.120 3 49358324 5 prime UTR variant G/A snv 0.29 0.28 3
rs5748469
TXNRD2
0.882 0.120 22 19919576 missense variant C/A snv 0.45 0.36 3
rs1656966 0.925 0.080 3 186748463 intron variant G/A snv 0.18 2
rs7745040 0.925 0.120 6 32696555 intergenic variant T/C snv 0.39 2
rs9275295 0.925 0.120 6 32695614 intergenic variant A/G snv 0.53 2
rs7033979
ASPN ; CENPP
0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs9473132
CD2AP
1.000 0.040 6 47554621 intron variant G/A;C snv 0.61 2
rs10842750
ITPR2
0.925 0.120 12 26537632 intron variant A/C;T snv 2
rs5746841
TXNRD2
0.925 0.040 22 19878161 missense variant C/A snv 2
rs1352815 1.000 0.040 14 80100388 intergenic variant C/A;T snv 1
rs1388382 1.000 0.040 14 80118358 intergenic variant G/A;C;T snv 1
rs7613610
ABI3BP
1.000 0.040 3 100780477 intron variant C/A snv 0.23 1
rs9850273
ABI3BP
1.000 0.040 3 100780521 intron variant G/A snv 0.31 1
rs1278300
ADAM12
1.000 0.040 10 126102615 intron variant A/G;T snv 1
rs11208030
ATG4C
1.000 0.040 1 62787158 intron variant G/A snv 0.17 1
rs12097658
ATG4C
1.000 0.040 1 62847648 intron variant T/C snv 0.15 1
rs4409690
ATG4C
1.000 0.040 1 62801139 intron variant G/A snv 0.18 1
rs6587988
ATG4C
1.000 0.040 1 62787095 intron variant C/T snv 0.26 1
rs142463796
COL10A1 ; NT5DC1
1.000 0.040 6 116121734 missense variant C/T snv 6.8E-03 2.2E-03 1
rs2228547
COL10A1 ; NT5DC1
1.000 0.040 6 116120483 missense variant C/A;G snv 1.2E-05; 0.14 1
rs2229783
COL11A1
1.000 0.040 1 102886895 missense variant A/C;G snv 0.59 1
rs6910140
COL9A1
1.000 0.040 6 70234554 missense variant T/C;G snv 3.9E-02 1