Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1473
PUM1
0.925 0.120 1 30940072 intron variant G/A snv 6.8E-02 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
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
rs1800247
BGLAP ; PMF1-BGLAP
0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
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
rs2047937
ZNF423
0.925 0.120 16 49830880 intron variant C/T snv 0.50 5
rs2178950
TRPS1
0.925 0.120 8 115640791 intron variant G/C snv 0.51 2
rs2239185
VDR
0.807 0.320 12 47850776 intron variant G/A snv 0.54 6
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2393799
P2RX7 ; LOC105370032
0.882 0.200 12 121132209 upstream gene variant C/A;T snv 3
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
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs3759579
MARK3
0.925 0.120 14 103384935 upstream gene variant A/G snv 0.55 2
rs3782905
VDR
0.882 0.200 12 47872384 intron variant G/C snv 0.29 3
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs4756846
SOX6
0.925 0.120 11 16381965 intron variant T/C snv 8.8E-02 2
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614