Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs12495941
ADIPOQ
0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs17366568
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1799941
SHBG
0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16