Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs73036519
EXOC3L2 ; MARK4
0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
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
rs11884770
COL4A3 ; MFF-DT
0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 4
rs181705462
CYP21A2 ; STK19
0.851 0.040 6 31979250 intron variant G/C;T snv 4
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 4
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 4
rs55975637
COL8A1
0.851 0.040 3 99701009 intron variant G/A;T snv 4
rs5817082
CETP
0.851 0.040 16 56963437 intron variant -/A delins 4
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 4
rs641153
CFB ; CYP21A2
0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 4
rs71507014
TRPM3
0.851 0.040 9 70823689 intron variant -/C;CC delins 4
rs79037040
TNFRSF10A ; LOC389641
0.807 0.160 8 23225458 non coding transcript exon variant G/A;C;T snv 4
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 4
rs2284665
HTRA1
0.882 0.040 10 122467114 intron variant G/A;T snv 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 2