Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs11061946
ADIPOR2
1.000 0.080 12 1719361 intron variant C/T snv 6.8E-02 2
rs11061973
ADIPOR2
1.000 0.080 12 1756770 intron variant G/A snv 0.12 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs13283456
PTGES2
0.925 0.080 9 128122474 missense variant C/A;T snv 4.0E-06; 0.13 3
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs137852787
PDX1
0.882 0.080 13 27924519 missense variant G/A snv 1.3E-03 2.0E-04 5
rs1486559930
FOLH1
11 49175866 missense variant A/G snv 4.0E-06 1
rs1527483
CD36
1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 2
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36