Disease: Serum HDL cholesterol measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000879
VIL1
2 218439407 intron variant G/A snv 4.1E-02 3
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 9
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 11
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 3
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 5
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs11216162
SIK3
11 116857561 non coding transcript exon variant G/A snv 0.17 3
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 7
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11570892
LPL
8 19966106 3 prime UTR variant A/G;T snv 3
rs11571111
REN
1 204161105 intron variant C/A snv 5.0E-03 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 6
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs11824953
MMP13
11 102949239 intron variant C/G snv 2.7E-02 3