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
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs765798193
PSMD9
0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs121434491
EFEMP1 ; LOC112268416
0.752 0.200 2 55871091 missense variant G/A snv 15
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs137853006
PROM1
0.776 0.080 4 16013299 missense variant G/A snv 11
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1557024919
HUWE1
0.925 0.240 X 53634235 splice donor variant C/G snv 7
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs62638634
RPGR
0.925 0.080 X 38322921 missense variant C/A snv 4
rs137853298
SYN3 ; TIMP3
0.925 0.080 22 32859351 missense variant A/T snv 3
rs281874657
COL4A5
0.925 0.160 X 108586717 stop gained C/T snv 3
rs12155400
HDAC9
7 18389298 intron variant A/G snv 2.9E-02 2
rs1249719
COL27A1
1.000 0.120 9 114235944 intron variant G/A snv 6.8E-02 2
rs281874727
COL4A5
1.000 0.160 X 108681837 stop gained C/T snv 2
rs2853502
ND5 ; CYTB
1.000 0.200 MT 13276 missense variant A/C;G;T snv 2
rs3751624
MYO5C
1.000 0.120 15 52282973 intron variant C/T snv 0.20 2