Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7