Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75527207
CFTR
0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs78655421
CFTR
0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs3813929
HTR2C
0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8