Disease: High density lipoprotein measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 28
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 6
rs605066 6 139508529 intron variant C/T snv 0.53 6