Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2521572
RAB3IL1
11 61944003 regulatory region variant T/G snv 0.91 1
rs2585617 6 68627895 non coding transcript exon variant A/G snv 0.90 1
rs6671200
TLCD4-RWDD3 ; LOC101928118
1 95231973 intron variant A/C snv 0.90 2
rs7942717
MIR6746 ; FADS3
11 61879816 intron variant G/A snv 0.89 2
rs2118674
MYO3B
2 170462384 intron variant A/T snv 0.87 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs6928281
SYCP2L
6 10908684 intron variant G/T snv 0.70 1
rs4465599
SHISA9
16 13061021 intron variant G/A snv 0.69 2
rs4713044
SYCP2L
6 10911049 intron variant G/A snv 0.68 1
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs422249 11 61872016 downstream gene variant T/C snv 0.67 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1061808
PPT2 ; EGFL8 ; AGPAT1 ; PPT2-EGFL8
6 32168770 3 prime UTR variant T/G snv 0.64 2
rs3134950
PPT2 ; PPT2-EGFL8
6 32159700 intron variant C/A snv 0.64 2
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs174456
FADS3
11 61888710 intron variant C/A snv 0.59 2
rs174464
FADS3
11 61890454 intron variant A/G snv 0.59 2
rs1225737
ELOVL2
6 10982419 3 prime UTR variant C/T snv 0.59 1
rs17675322
ELOVL2-AS1
6 11058952 intron variant T/A snv 0.59 1
rs9295764
ELOVL2 ; ELOVL2-AS1
6 11044963 non coding transcript exon variant A/G snv 0.59 1
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs4711146
SYCP2L
6 10961172 intron variant T/C snv 0.58 1