Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239185
VDR
0.807 0.320 12 47850776 intron variant G/A snv 0.54 6
rs2047937
ZNF423
0.925 0.120 16 49830880 intron variant C/T snv 0.50 5
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs1800247
BGLAP ; PMF1-BGLAP
0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02 3
rs2393799
P2RX7 ; LOC105370032
0.882 0.200 12 121132209 upstream gene variant C/A;T snv 3
rs3782905
VDR
0.882 0.200 12 47872384 intron variant G/C snv 0.29 3
rs1473
PUM1
0.925 0.120 1 30940072 intron variant G/A snv 6.8E-02 2
rs1554606
IL6 ; IL6-AS1
0.925 0.120 7 22729088 intron variant T/A;G snv 2
rs17277372
DNM3
0.925 0.120 1 172218334 intron variant A/G snv 0.22 2
rs2178950
TRPS1
0.925 0.120 8 115640791 intron variant G/C snv 0.51 2
rs297325
SOX6
0.925 0.120 11 16368048 intron variant T/C;G snv 2
rs335170
PRDM6
0.925 0.120 5 123146549 intron variant A/C;G;T snv 2
rs3759579
MARK3
0.925 0.120 14 103384935 upstream gene variant A/G snv 0.55 2
rs4756846
SOX6
0.925 0.120 11 16381965 intron variant T/C snv 8.8E-02 2
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv 2