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
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs750359414
RETN
0.851 0.240 19 7669884 missense variant C/G;T snv 4.0E-06; 4.0E-06 5
rs45539933
UCP1
0.882 0.280 4 140567914 missense variant C/T snv 8.7E-02 7.7E-02 5
rs16995309
PTPN1
0.882 0.280 20 50581336 missense variant C/T snv 4.8E-03 5.0E-03 4
rs622342
SLC22A1
0.882 0.280 6 160151834 intron variant C/A snv 0.70 4
rs1466929132
SLCO1A2 ; IAPP
0.925 0.200 12 21378325 missense variant G/A;C snv 4.0E-06 3
rs374057152
VEGFA
0.925 0.200 6 43777592 missense variant T/C snv 4.0E-06 1.4E-05 3
rs1871922
CNBP ; LOC105374101
1.000 0.120 3 129183756 intron variant G/C;T snv 1
rs1303471186
SCN4A
1.000 0.120 17 63972627 missense variant G/A;T snv 2.5E-05; 4.2E-06 1