Disease: Serum total cholesterol 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
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 3
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
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 4
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6
rs10438978
LOC105372112
18 49631816 intergenic variant T/C snv 0.75 2
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs10744826
UBE3B
12 109527707 intron variant C/G snv 0.57 3
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
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
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
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10 2
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4
rs112545201
ETV5
3 186085743 intron variant C/T snv 0.14 3
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5