Source: INFERRED ×
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
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 14
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 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
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 11
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 10
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 10
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10