Disease: High density lipoprotein measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000879
VIL1
2 218439407 intron variant G/A snv 4.1E-02 3
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs1009360
LOC107984063 ; LINC02245 ; LINC02576
2 65048915 intron variant T/C snv 0.51 2
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs10713774 4 26048829 intergenic variant C/- del 0.18 3
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 5
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 5
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs10864728
GALNT2
1 230169168 intron variant A/G snv 0.50 3
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4
rs11216162
SIK3
11 116857561 non coding transcript exon variant G/A snv 0.17 3
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs112875651 8 125494452 intron variant G/A snv 0.31 7