Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2257129
LOC105378522
1.000 0.040 10 121139183 regulatory region variant T/C snv 0.82 3