Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1040922 20 10787163 intron variant G/T snv 0.27 1
rs10427021
INSR
19 7259335 intron variant T/C;G snv 0.15 2
rs10458896
KIF18A
11 28036410 missense variant T/C snv 0.31 0.38 1
rs10468291
ZNF423
16 49734135 intron variant C/A snv 0.64 1
rs1047030
SORBS3
8 22571195 missense variant A/G snv 0.18 0.16 1
rs10504249
LINC01602 ; LOC105375856
8 57876522 intron variant A/G snv 1.7E-02 3
rs1053711
SLMAP
3 57757519 5 prime UTR variant G/A snv 0.22 1
rs1060105
SBNO1
0.925 0.120 12 123321672 missense variant C/T snv 0.19 0.16 3
rs10628234 15 74918801 downstream gene variant -/CA delins 2
rs1063281
TNS1
2 217804009 3 prime UTR variant C/A;T snv 2
rs10743353
LINC02398
12 20047028 intron variant C/T snv 0.60 2
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs10747570
COX14
12 50116154 intron variant A/C;G;T snv 2
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs10751962 10 4130519 intergenic variant C/G;T snv 1
rs10761530
ANK3
10 60630968 intron variant T/C snv 0.51 1
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs1081707 2 96381261 downstream gene variant G/A snv 0.24 1
rs10822407 10 65024342 intergenic variant T/C snv 0.30 1
rs10850519
LOC105370003
12 115490635 intergenic variant G/C snv 0.22 1
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10858948
LOC105369890
12 90084874 intron variant G/A snv 0.51 2
rs10864859 2 120682642 downstream gene variant G/C;T snv 1
rs10873612
ATP10A
15 25860455 intron variant C/T snv 0.45 1