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
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
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
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 3
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 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
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 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
rs11340914
TCEA3
1 23421504 intron variant AA/-;A;AAA delins 0.65 2
rs115485095
CYP21A2 ; EHMT2
6 31888293 intron variant G/A snv 3
rs115845232
LOC112267902 ; HLA-B
6 31304484 intron variant C/T snv 3
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv 3
rs116477171
CYP21A2 ; C2
6 31918153 intron variant C/G;T snv 3
rs11652146
ZNF652
17 49345001 intron variant G/A;C snv 4
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 4
rs118146573
CETP
16 56967026 intron variant G/A snv 9.4E-02 3
rs11987974
LOC105379376
8 36966299 intergenic variant C/A;T snv 4