Source: GWASDB ×
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 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs10754187
KCNT2
1.000 0.040 1 196447122 intron variant A/G;T snv 2
rs10801532
KCNT2
1.000 0.040 1 196395046 intron variant A/G;T snv 2
rs10801551 1.000 0.040 1 196610909 upstream gene variant G/A;C snv 2
rs10922144 1.000 0.040 1 196854170 intron variant C/A;T snv 2
rs12124794
CFH
1.000 0.040 1 196692408 intron variant A/G;T snv 2
rs12755054
CFHR5
1.000 0.040 1 196977900 intron variant T/A;C snv 2
rs1963605 1.000 0.040 1 196853038 intron variant C/A;T snv 2
rs1964645 1.000 0.040 1 196852884 intron variant T/A;C snv 2
rs2284664
CFH
0.925 0.040 1 196733395 intron variant C/A;T snv 2
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 2
rs4657825 1.000 0.040 1 196615191 intergenic variant A/G;T snv 2
rs4915318
LOC105371675
1.000 0.040 1 196927958 intergenic variant C/A;T snv 2
rs4915559
CFHR4 ; LOC105371675
1.000 0.040 1 196917640 intron variant T/A;C snv 2
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 2
rs10510109 1.000 0.040 10 122360941 intergenic variant G/A;T snv 1
rs10733086
CFH
1.000 0.040 1 196707805 intron variant A/C;T snv 1
rs10801575 1.000 0.040 1 196883651 intron variant T/A;C snv 1
rs10887142 1.000 0.040 10 122347969 downstream gene variant G/A;C snv 1
rs10887149
PLEKHA1
1.000 0.040 10 122407488 intron variant G/A;C snv 1
rs10922083
KCNT2
1.000 0.040 1 196547268 intron variant C/A;T snv 1