Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs9836225
MGLL
3 127797551 intron variant C/T snv 7.4E-03 3
rs7666097
KDR
4 55124971 intron variant T/A;C snv 5
rs11960617
SGCD
5 156494033 intron variant C/T snv 1.9E-02 3
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs17513478
RIPK1
6 3101321 intron variant G/A snv 5.7E-03 5
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04 3
rs2975634
NOD1
7 30452077 missense variant C/A;T snv 4.0E-06; 6.3E-03 3
rs7811025 7 99788078 upstream gene variant C/T snv 4.8E-02 4
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
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
rs2954031 8 125479491 intron variant G/T snv 0.42 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs2980869 8 125476008 intron variant C/T snv 0.48 6