Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs2082940
ADIPOQ-AS1 ; ADIPOQ
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs2229569
SELL ; C1orf112
0.790 0.360 1 169704697 missense variant G/A;T snv 0.21; 3.2E-05 8
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 8
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs1056534
FN3K ; TBCD
0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs2075241
LRP6 ; BCL2L14
0.882 0.200 12 12138545 intron variant G/A;C snv 0.18 4
rs56094641
FTO
0.925 0.160 16 53772541 intron variant A/G;T snv 4
rs61758388
LOC107987234 ; XYLT1
0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs6504649
XYLT2
0.882 0.280 17 50360095 missense variant C/G;T snv 0.33; 3.2E-05 4
rs117897666
LOC105370892
0.882 0.160 15 73811619 intergenic variant C/T snv 3
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs1411766
LOC101927627
0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs55703767
MFF-DT ; COL4A3
0.925 0.160 2 227256385 missense variant G/A;T snv 4.0E-06; 0.17 3
rs11538209
ALB
1.000 0.120 4 73404356 missense variant T/C snv 2
rs1531343
RPSAP52
0.925 0.160 12 65781114 intron variant G/C;T snv 2
rs17300593 0.925 0.160 1 58637536 intergenic variant C/G snv 2
rs491347
LRP5
0.925 0.200 11 68402220 intron variant G/A;T snv 2
rs994411260
DNMT1
0.925 0.160 19 10194877 missense variant G/C snv 2
rs9966483
LOC643542
0.925 0.160 18 67783109 intron variant G/A;T snv 2