Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 7
rs7961581
TSPAN8
0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs4753426
MTNR1B
0.827 0.280 11 92968430 upstream gene variant T/C snv 0.49 6