Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 2
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 2
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 2
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs2000813
LIPG
0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 1
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 2
rs37369
AGXT2
0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 1
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2075674
TFR2
1.000 0.040 7 100627408 synonymous variant G/A snv 0.18 0.16 1
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 3
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 5
rs6046
F7
0.925 0.080 13 113118845 missense variant G/A;C;T snv 0.13 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20