Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1991517
LOC101928462 ; TSHR
0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs3789604
RSBN1 ; AP4B1-AS1
0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs4416670 0.827 0.240 6 43982716 intergenic variant T/C snv 0.45 7
rs121908873
TSHR ; LOC101928462
0.790 0.160 14 81139828 missense variant G/A;T snv 7
rs121908874
TSHR ; LOC101928462
0.807 0.080 14 81143584 missense variant T/C snv 7
rs3827440
GPR174 ; LOC107985690
0.851 0.120 X 79171491 missense variant T/A;C snv 5.5E-06; 0.51 6
rs2046045
PDE8B
0.925 0.080 5 77239986 intron variant T/C;G snv 4
rs28937584
TSHR ; LOC101928462
0.925 0.080 14 81143955 missense variant G/A;C snv 4.0E-06 4
rs1311839715
KCNJ18
0.882 0.200 17 21703291 missense variant G/C snv 7.0E-06 3
rs571893270
LOC101928462 ; TSHR
0.882 0.040 14 81143641 missense variant G/A snv 8.0E-05 2.1E-05 3
rs12138950
LOC105376817 ; LOC105376819 ; LOC105376818 ; MICOS10
0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 3
rs9355610
LOC105378120
0.882 0.200 6 166969587 downstream gene variant G/A;T snv 3
rs12722039
HLA-DQA2 ; HLA-DQA1 ; LOC107986589
0.925 0.120 6 32637507 missense variant G/A snv 5.7E-02 8.4E-02 2
rs121908879
LOC101928462 ; TSHR
0.925 0.080 14 81096641 missense variant A/G snv 2
rs2983514
PDE10A
0.925 0.040 6 165636631 intron variant A/G snv 0.34 2
rs925488
PTCSC2
1.000 0.040 9 97784109 intron variant G/A snv 0.71 2
rs1482760341
SOD1 ; SCAF4
0.925 0.120 21 31668548 missense variant G/C;T snv 1.6E-05 2
rs118039499
TMEM71
1.000 0.040 8 132759389 5 prime UTR variant A/C snv 1.4E-02 2
rs121908875
TSHR ; LOC101928462
0.925 0.040 14 81144073 missense variant G/A snv 2
rs17477923
FAM227B
1.000 0.040 15 49418988 intron variant T/C snv 0.22 1
rs8077245
LINC00511
1.000 0.040 17 72380036 intron variant G/T snv 0.63 1