Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057972
IL15
0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs1194197
CD36
0.925 0.080 7 80546290 intron variant A/G snv 0.52 2
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1414334
HTR2C
0.851 0.160 X 114903581 intron variant C/G snv 5
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs17373080
NR1H2
0.851 0.160 19 50376267 5 prime UTR variant C/G snv 0.29 4
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1799941
SHBG
0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121