Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174538
TMEM258 ; MIR611 ; FEN1
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6