Disease: Serum HDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs34183407
ALMS1
2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8