Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
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
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 10
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 9
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 8