Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs8020333
FOXN3
14 89568505 intron variant C/G;T snv 0.52 2
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs17762454
RREB1
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs4869272
MIR583HG ; LOC101929710
5 96203744 intron variant C/T snv 0.72 3
rs10500292
SYMPK
19 45824675 intron variant C/T snv 0.46 2
rs11039130 11 47207765 intergenic variant C/T snv 0.20 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs2280231
KBTBD4 ; NDUFS3
11 47578886 5 prime UTR variant C/T snv 0.24 0.20 2
rs35859536
LOC105375716
8 117179236 downstream gene variant C/T snv 0.25 2
rs4775471 15 62132450 intergenic variant C/T snv 0.18 2
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 5