Disease: Serum total cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 8
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4