Disease: Metabolic Syndrome X
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 12
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 12
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 11
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 11
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 10
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 9
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 8
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 8
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 8
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7