Disease: High density lipoprotein measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 2
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs10713774 4 26048829 intergenic variant C/- del 0.18 3
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1145198 11 116703620 intergenic variant G/A snv 0.21 2
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs11940232 4 137812732 intron variant C/T snv 0.22 2
rs11967262 6 43792590 intergenic variant C/G snv 0.41 4
rs11984636 8 20028215 intergenic variant T/C snv 8.3E-02 2
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 5
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 3
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 8
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8