Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2288775
NEDD4L
1.000 0.040 18 58316132 intron variant A/G snv 0.25 2
rs2918419
NR3C1
0.925 0.040 5 143342788 intron variant T/C snv 0.15 2
rs2963791 1.000 0.040 5 3844427 regulatory region variant C/A snv 0.80 2
rs359935 1.000 0.040 1 89517625 intron variant G/A;T snv 2
rs3733591
SLC2A9
0.925 0.040 4 9920506 missense variant C/T snv 0.25 0.17 2
rs3757840
GCK
1.000 0.040 7 44191617 intron variant T/C;G snv 2
rs3816117
CETP
1.000 0.040 16 56962246 5 prime UTR variant T/C snv 0.52 2
rs3937443
POU6F2 ; LOC105375238
1.000 0.040 7 39474399 intron variant T/C snv 0.77 2
rs4387351
EML3 ; ROM1
1.000 0.040 11 62613260 5 prime UTR variant T/C snv 0.98 0.94 2
rs470117
CPT1B ; CHKB-CPT1B
1.000 0.040 22 50571524 missense variant C/T snv 0.42 0.36 2
rs4922117 1.000 0.040 8 19995075 regulatory region variant T/A;C;G snv 0.25 2
rs495348
ALDH1A2
1.000 0.040 15 58395591 intron variant C/G snv 0.82 2
rs496300
LINC01679
1.000 0.040 21 43359800 intron variant C/T snv 0.73 2
rs561005732
GGT1
0.925 0.040 22 24627519 missense variant A/C;G snv 8.0E-06 2
rs569805
ABCB11
1.000 0.040 2 168926370 intron variant A/T snv 0.73 2
rs603446
ZPR1
1.000 0.040 11 116783719 intron variant C/T snv 0.33 2
rs6439106
MGLL
1.000 0.040 3 128000111 intron variant C/T snv 0.13 2
rs6585514 1.000 0.040 10 118836874 intron variant A/G snv 0.62 2
rs658995
CBLN2
1.000 0.040 18 72540105 non coding transcript exon variant A/G;T snv 2
rs6711016 1.000 0.040 2 20923592 intergenic variant C/A snv 0.19 2
rs675
APOA4
1.000 0.040 11 116820959 missense variant T/A;C snv 0.15; 1.2E-03 2
rs6887452
IL17B
1.000 0.040 5 149404204 upstream gene variant T/G snv 0.32 2
rs759364715
GIPR
1.000 0.040 19 45672880 missense variant G/A snv 2.0E-05 2.1E-05 2
rs7865146 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 2
rs8060686
EDC4
1.000 0.040 16 67877614 synonymous variant T/C snv 0.23 0.32 2