Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs1223493898
HNF4A
0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 5
rs13154178
SELENOP
5 42827999 intron variant G/A snv 0.31 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs1366600
INSR
1.000 0.080 19 7112870 3 prime UTR variant A/G snv 5.9E-02 2
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