Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6