Disease: Low density lipoprotein cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs10986881
PBX3
9 125756807 intron variant C/T snv 1.8E-02 3
rs7100433
ECHS1
10 133370298 intron variant T/C snv 0.98 3
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs5185
AGTR1
3 148742185 3 prime UTR variant T/G snv 6.7E-03 2.5E-02 4
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 4
rs876528
ADRA1B
5 159964639 intron variant G/A snv 2.3E-02 3
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs5743316
TLR3
4 186082537 missense variant A/T snv 4.0E-05 3.5E-05 3
rs8176445
TFPI ; LOC105373786
2 187498080 intron variant T/C snv 8.7E-03 4
rs7951347
CSRP3 ; CSRP3-AS1
11 19198031 intron variant T/A;C snv 3
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 5
rs2238675
NCAN
19 19225799 intron variant C/T snv 9.4E-02 4
rs8105094
HAPLN4
19 19263252 intron variant C/T snv 0.19 4
rs2023883
SUGP1
19 19294671 intron variant G/A snv 0.19 4
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs1859287
SUGP1
19 19311378 intron variant T/A;C;G snv 4
rs2285628
MAU2
19 19357187 3 prime UTR variant T/A snv 0.22 4
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs4808199
GATAD2A ; MIR640
1.000 0.040 19 19434290 intron variant G/A;T snv 0.19 4
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3