Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11