Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs12394306
SYN1
X 47576648 splice region variant A/C;T snv 4.3E-03 4
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2255141
GPAM
10 112174128 intron variant A/G;T snv 5
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 4
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs7666097
KDR
4 55124971 intron variant T/A;C snv 5
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs9341059
ESR1
6 152097101 intron variant C/A;T snv 4