Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
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
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs767910122
KCNH2
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448
KCNH2
0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38 10
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs11571836
BRCA2
0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs225015
DIO2
0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs199473244
SCN5A
0.851 0.120 3 38557251 missense variant C/A snv 4
rs1050286
OLR1
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3