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
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs9565177
LMO7 ; LMO7-AS1
1.000 0.120 13 75621267 5 prime UTR variant T/G snv 0.19 1
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs833069
VEGFA
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs3007729 1.000 0.120 1 18468761 regulatory region variant T/C;G snv 1
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs1549758
NOS3
0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs17366743
ADIPOQ-AS1 ; ADIPOQ
0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02 7
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs3025021
VEGFA
0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 4
rs9362054
LOC107986620 ; LINC01611
0.882 0.160 6 84468550 intron variant T/C snv 0.52 3
rs3913535
NOX4
0.925 0.160 11 89363589 intron variant T/C snv 0.30 2
rs4462262 0.925 0.120 10 57429418 intergenic variant T/C snv 0.55 2
rs6060566
NFS1 ; ROMO1
0.925 0.160 20 35700304 intron variant T/C snv 0.19 2
rs1043045
SLMAP
1.000 0.120 3 57928451 3 prime UTR variant T/C snv 0.31 1
rs2070682
SERPINE1
1.000 0.120 7 101133986 intron variant T/C snv 0.44 1
rs227455 1.000 0.120 6 165064562 intron variant T/C snv 0.17 1
rs2811893
MYSM1
1.000 0.120 1 58696476 intron variant T/C snv 0.39 1
rs3783028
UCHL3
1.000 0.120 13 75591146 intron variant T/C snv 0.77 1
rs6856425
SLC26A1 ; DGKQ
1.000 0.120 4 983130 intron variant T/C snv 7.6E-02 1
rs75360147
SLC28A3
1.000 0.120 9 84349773 intron variant T/C snv 2.4E-02 1
rs772346653
VIP
1.000 0.120 6 152752206 missense variant T/C snv 8.0E-06 1