Disease: Serum total cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9