Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7048601
TEX10
9 100311981 intron variant G/T snv 0.63 1
rs11160601 14 100720304 regulatory region variant C/G;T snv 1
rs775327225 X 100764930 intergenic variant T/C snv 5.3E-04 1
rs11597119
SLF2
10 100914591 intron variant A/G snv 0.35 1
rs2643672
LOC105369944
12 102648521 intergenic variant G/A;C snv 1
rs139055636 9 102796618 regulatory region variant C/A;T snv 1
rs2923097
CAND1.11 ; AMPD3
11 10343497 intron variant A/G;T snv 1
rs2726491
TET2-AS1
4 105291405 upstream gene variant G/A snv 0.27 2
rs191578361
GCNT2
6 10606778 intron variant C/A snv 4.8E-03 1
rs2163832
SLC44A2
19 10635088 intron variant T/A;C;G snv 0.73; 4.0E-06 1
rs6477547
ZNF462
9 106882584 intron variant C/T snv 0.43 1
rs9398171
FOXO3
1.000 0.040 6 108662324 intron variant C/T snv 0.55 2
rs16892496
TRHR
1.000 0.080 8 109097622 intron variant A/C;G;T snv 2
rs7832552
TRHR
8 109103447 intron variant C/T snv 0.29 1
rs1541597 12 109607113 intergenic variant G/T snv 0.20 1
rs1884429 1 11052779 downstream gene variant T/C snv 0.74 2
rs1345203
SOCAR ; MIR4435-2HG
2 111496274 intron variant T/C;G snv 2
rs2737218
TRPS1
8 115619051 intron variant T/C snv 0.23 1
rs9866470
VGLL4
3 11588003 intron variant C/G;T snv 1
rs7027103
PAPPA
9 116363822 intron variant G/C snv 0.16 1
rs2900208
ETV6
12 11725530 intron variant C/A snv 0.29 2
rs2474944 1 118342903 intergenic variant T/A;C;G snv 1
rs607472 11 118809363 regulatory region variant C/G snv 0.41 1
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3