Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs5817082
CETP
0.851 0.040 16 56963437 intron variant -/A delins 4
rs58978565
TNR
0.882 0.040 1 175376466 intron variant -/AGAGT ins 0.37 3
rs71507014
TRPM3
0.851 0.040 9 70823689 intron variant -/C;CC delins 4
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs9621532
SYN3
0.851 0.040 22 32688525 intron variant A/C snv 5.8E-02 4
rs75165563
EXOC5
0.925 0.040 14 57220928 intron variant A/C snv 4.5E-04 2
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 5
rs11775442
ANGPT2 ; MCPH1
0.925 0.040 8 6538837 intron variant A/G snv 0.20 2
rs754100400
IGFN1
0.925 0.040 1 201211089 missense variant A/G snv 7.1E-06 4.6E-05 2
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs3173800
CD36
0.925 0.040 7 80660605 intron variant A/T snv 0.29 2
rs4455855
MCPH1 ; ANGPT2
0.925 0.040 8 6539909 intron variant A/T snv 0.57 2
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13