Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5
rs267606841
GALNT3
0.882 0.120 2 165749801 missense variant A/C snv 5
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs3862434
CRTC3
1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs1917760
LOC105375545 ; GSTK1 ; LOC105375546
7 143262206 intron variant G/A;T snv 1.8E-02 1
rs5767700
PPARA
22 46216775 intron variant T/C;G snv 1
rs5767743
PPARA
22 46226097 intron variant T/C snv 0.36 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1799904
LOC101929710 ; PCSK1
1.000 0.080 5 96429259 missense variant C/A;T snv 4.0E-06; 2.1E-03 2