Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11075986
FTO
1.000 0.080 16 53771432 intron variant C/G snv 0.15 1
rs11075987
FTO
1.000 0.080 16 53781249 intron variant T/A;G snv 0.59 2
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11076023
FTO
0.925 0.120 16 54118136 3 prime UTR variant A/T snv 0.49 2
rs1107756
APPL2 ; C12orf75
1.000 0.080 12 105235461 intron variant A/G snv 0.33 1
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs11088859
NCAM2
1.000 0.080 21 21317024 intron variant G/A snv 4.5E-02 1
rs1109859
PEMT
1.000 0.080 17 17521019 intron variant G/A snv 0.83 1
rs11109072
RMST
1.000 0.080 12 97507492 intron variant C/A snv 0.12 1
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 2
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs11202222
BMPR1A
1.000 0.080 10 86842729 intron variant C/G snv 0.18 1
rs11202592
KLLN ; PTEN
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs11205591 1.000 0.080 1 39035577 downstream gene variant C/G;T snv 1
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 2
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1126680
BCHE
0.851 0.160 3 165837337 synonymous variant C/T snv 5.6E-02 5.6E-02 5
rs1127568
ADCY3
1.000 0.080 2 24823221 synonymous variant T/C;G snv 0.69; 4.0E-06 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136287
SERPINF1
0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29