Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908525
AGXT
0.790 0.160 2 240875159 missense variant T/C snv 4.4E-05 5.6E-05 7
rs121908529
AGXT
0.851 0.160 2 240871433 missense variant G/A;C snv 5.6E-04 4
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs12197043 0.882 0.160 6 149130141 regulatory region variant A/G snv 0.37 3
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12431381
RTN1
0.925 0.080 14 59643053 intron variant T/C snv 0.35 2
rs12434215
RTN1
0.882 0.160 14 59642862 intron variant A/G snv 0.33 3
rs12437854
LOC107983974
0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs13447075
PVT1
0.882 0.120 8 127998344 non coding transcript exon variant C/A snv 4
rs1372834938
KIDINS220
0.763 0.280 2 8812465 missense variant G/C snv 4.2E-06 12
rs138924661
DGKE ; TRIM25
0.807 0.120 17 56848773 stop gained G/A snv 9.1E-05 1.5E-04 9
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs143810759
LIG4
0.851 0.280 13 108210371 missense variant C/T snv 1.6E-04 2.1E-04 6
rs1452199941
TBC1D9
0.827 0.160 4 140670787 missense variant T/C snv 7.0E-06 5
rs145640112
KLKB1
0.925 0.080 4 186250267 missense variant A/C;G snv 1.8E-04; 4.0E-06 2
rs146400394
NPHS1
0.925 0.080 19 35842486 missense variant C/T snv 6.8E-05 4.9E-05 2