Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 4
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 4
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs11884770
COL4A3 ; MFF-DT
0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs12038333
CFH
1.000 0.040 1 196703324 intron variant G/A snv 0.64 1
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 1
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 4
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs12498917 1.000 0.040 4 40302730 intergenic variant A/T snv 5.0E-02 1
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 2
rs12661281
SLC44A4 ; CYP21A2
0.882 0.040 6 31874821 missense variant T/A snv 0.15 0.11 2
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 3
rs12887388
DPF3
1.000 0.040 14 72863136 intron variant G/A snv 0.64 1
rs12930861 1.000 0.040 16 10492245 upstream gene variant C/A;G;T snv 1
rs13081855
COL8A1
1.000 0.040 3 99762695 intron variant G/T snv 8.0E-02 1
rs13278062
LOC389641 ; TNFRSF10A
0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 1
rs1329424
CFH
1.000 0.040 1 196677046 non coding transcript exon variant T/G snv 0.66 1
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 3
rs139161960 1.000 0.040 5 29538059 intergenic variant T/G snv 0.10 1
rs140647181
LOC105374007
0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5