Disease: Triglycerides measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs3177928
HLA-DRA
0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 8
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7