Disease: High density lipoprotein measurement
Source: GWASCAT ×
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
rs1009360
LOC107984063 ; LINC02245 ; LINC02576
2 65048915 intron variant T/C snv 0.51 2
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 2
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
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 3
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 4
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs10808546 8 125483576 intron variant C/T snv 0.39 6
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