Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62048402
FTO
0.882 0.200 16 53769311 intron variant G/A snv 0.31 3
rs13188458 0.882 0.160 5 8127718 intergenic variant T/G snv 0.22 4
rs7713645
PIK3R1
0.851 0.200 5 68231498 intron variant A/C snv 0.58 4
rs2075356
GHRL ; GHRLOS
0.882 0.160 3 10287125 non coding transcript exon variant T/C snv 8.3E-02 5
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs1800234
PPARA
0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs572169
GHSR
0.882 0.160 3 172447937 synonymous variant C/T snv 0.31 0.24 6
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 7
rs7566605
LOC107985940
0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28