Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs2297991
GPAM
10 112153464 3 prime UTR variant T/C snv 0.69 4
rs77147124
GPAM
10 112159366 intron variant A/G snv 4
rs2255141
GPAM
10 112174128 intron variant A/G;T snv 4
rs2803621
GPAM
10 112179826 intron variant G/A snv 0.74 4
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 5
rs2384034
RPH3A
12 112766880 intron variant C/G;T snv 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs2367970 11 116710925 intergenic variant G/A snv 0.22 3