Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2692695
TF
1.000 0.080 3 133766610 intron variant A/G snv 0.56 2
rs28581706
ULK4
1.000 0.160 3 41829905 intron variant A/C;T snv 2
rs4525863
TF ; INHCAP
1.000 0.080 3 133717292 intron variant C/A snv 0.32 2
rs62258655
ULK4
1.000 0.160 3 41890838 intron variant G/A snv 0.11 2
rs7638018
TF
1.000 0.040 3 133776617 intron variant A/G snv 0.29 2
rs8177272
TF
1.000 0.040 3 133764026 intron variant G/A snv 0.29 2
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs881844
STARD3
0.925 0.080 17 39653965 intron variant C/G snv 0.51 4
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 3
rs8177178
TF ; INHCAP
0.925 0.080 3 133744428 intron variant G/A snv 0.33 3
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 4
rs1830084
SRPRB ; LOC105374116 ; TF
0.882 0.160 3 133789620 3 prime UTR variant A/G;T snv 4