Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs760242
DHCR7
11 71435530 missense variant C/T snv 2.2E-04 6.3E-05 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs7993724
PDX1 ; PLUT
13 27919139 upstream gene variant T/C snv 5.6E-03 6
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs7756521
DDR1
1.000 6 30880476 intron variant T/C snv 0.25 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs4704220
CERT1
5 75461731 intron variant G/A snv 0.55 5