Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs438811
APOC1
19 44913484 non coding transcript exon variant C/T snv 0.29 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4
rs11652146
ZNF652
17 49345001 intron variant G/A;C snv 4
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 4
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4