Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs146695489
ABCC8
0.925 0.160 11 17470170 missense variant T/C snv 2.5E-04 5.6E-05 2
rs2014355
ACADS
0.925 0.120 12 120737721 non coding transcript exon variant T/C snv 0.22 4
rs9997745
ACSL1
0.925 0.040 4 184816689 intron variant G/A snv 0.25 2
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs148969251
ARHGEF12
1.000 0.040 11 120480110 missense variant A/G snv 3.3E-02 1.3E-02 1
rs886041065
ASXL2
0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs4629571
CERT1 ; HMGCR
0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02 2
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs225017
DIO2
0.925 0.080 14 80200883 3 prime UTR variant A/T snv 0.58 2
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs121909731
GLUD1
0.851 0.120 10 87057692 missense variant G/A;C snv 4.0E-06 7
rs121909730
GLUD1
0.882 0.040 10 87053380 missense variant G/A snv 4
rs193922479
HNF4A
0.925 0.080 20 44424116 missense variant C/A;T snv 8.0E-06 7.0E-06 2