Disease: Triglycerides measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 6
rs11743303
C5orf67
5 56564125 intron variant A/G snv 0.21 2
rs2222328
IQCJ-SCHIP1 ; SCHIP1
3 159541502 intron variant T/C snv 0.17 2