Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11611206
LOC105369818 ; MDM1
0.851 0.200 12 68274666 intron variant G/A snv 0.15 4
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 4
rs17759659
BCL2
0.851 0.120 18 63291411 intron variant A/G snv 0.31 4
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs3816769
STAT3
0.851 0.240 17 42346255 intron variant T/A;C snv 4
rs7085433
TIMM23
1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 4
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 3
rs1800591
MTTP
0.882 0.120 4 99574331 intron variant G/T snv 0.26 3
rs2071400
TPO
0.882 0.120 2 1412867 intron variant C/T snv 0.11 3
rs2291282
STAT3
0.882 0.120 17 42346547 intron variant T/C snv 1.2E-03 3.4E-04 3
rs7537605
VAV3
0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs7629750
TMEM39A
0.882 0.040 3 119455829 intron variant A/G snv 0.45 3
rs11935941
LOC107986195
1.000 0.040 4 148731326 intron variant A/C snv 0.31 2
rs12101255
TSHR
0.925 0.120 14 80984708 intron variant C/T snv 0.37 2
rs1269486
GATA3 ; GATA3-AS1 ; LOC107984204
0.925 0.120 10 8054236 intron variant A/G snv 0.77 2
rs2184658
HLX-AS1 ; HLX
0.925 0.120 1 220879115 intron variant C/G snv 0.20 2
rs2268458
TSHR
0.925 0.120 14 80996551 intron variant T/C snv 0.20 2
rs3783938
TSHR ; LOC101928462
0.925 0.120 14 81128036 intron variant C/T snv 0.13 2
rs4411444
TSHR
0.925 0.120 14 80978764 intron variant A/G snv 0.43 2
rs4903961
TSHR
0.925 0.120 14 80996305 intron variant C/G snv 0.39 2
rs5998672
UBE2L3
0.925 0.120 22 21612153 intron variant G/A snv 0.31 2
rs756763
CA10
1.000 0.040 17 51671952 intron variant A/G snv 0.48 2
rs12730735
AP4B1-AS1 ; PTPN22
1.000 0.040 1 113838835 intron variant T/C snv 0.21 1
rs165501
IRAK2
1.000 0.040 3 10167559 intron variant T/A;C snv 1