Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7094463
TCF7L2
10 112952224 intron variant A/G snv 0.57 1
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10802502
NLRP3
1 247448993 3 prime UTR variant C/T snv 0.55 1
rs7598922
DHX57
2 38855202 missense variant T/C snv 0.62 0.54 1
rs8111699
STK11
0.851 0.200 19 1209715 intron variant C/G snv 0.53 6
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs3741845
TAS2R9
12 10809516 missense variant A/G snv 0.60 0.51 1
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4753426
MTNR1B
0.827 0.280 11 92968430 upstream gene variant T/C snv 0.49 6
rs7929804
KCNQ1OT1 ; KCNQ1
11 2619594 non coding transcript exon variant G/A snv 0.49 1
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs4721
LRRC61 ; RARRES2
1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47 2
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 4
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 5
rs1042531
PCK1
20 57565924 3 prime UTR variant T/G snv 0.45 1
rs231841
KCNQ1
11 2702374 intron variant G/T snv 0.45 1
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs351219
STRA6
15 74196866 intron variant T/C snv 0.44 1
rs2236745
PCK1
20 57561937 non coding transcript exon variant T/C snv 0.44 1
rs9645501
LOC101928994 ; HKDC1
10 69227010 intron variant G/A snv 0.43 1
rs275645 3 148746667 downstream gene variant G/A snv 0.43 1
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157