Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs5817082
CETP
0.851 0.040 16 56963437 intron variant -/A delins 4
rs71507014
TRPM3
0.851 0.040 9 70823689 intron variant -/C;CC delins 4
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs1831282
CFH
1.000 0.040 1 196704863 intron variant A/C snv 0.62 2
rs1061147
CFH
1.000 0.040 1 196685194 synonymous variant A/C snv 0.68 0.62 1
rs10801553
CFH
1.000 0.040 1 196686613 intron variant A/C snv 0.64 1
rs17073641 1.000 0.040 18 64751208 intergenic variant A/C snv 0.41 1
rs9621532
SYN3
0.851 0.040 22 32688525 intron variant A/C snv 5.8E-02 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1064583
NT5DC1 ; COL10A1
0.925 0.040 6 116125413 missense variant A/C;G snv 0.37 1
rs17050244 1.000 0.040 2 120525054 regulatory region variant A/C;G snv 1
rs2839127
FTCD
1.000 0.040 21 46153636 intron variant A/C;G snv 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs10733086
CFH
1.000 0.040 1 196707805 intron variant A/C;T snv 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 4
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 4
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 3
rs10922106
CFH
0.925 0.080 1 196722334 intron variant A/G snv 0.43 2
rs10754199
CFH
1.000 0.040 1 196701709 intron variant A/G snv 0.64 1