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
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 5
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs11216162
SIK3
11 116857561 non coding transcript exon variant G/A snv 0.17 3
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
rs11824953
MMP13
11 102949239 intron variant C/G snv 2.7E-02 3
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs11856159
ALDH1A2
15 58406811 intron variant C/A;G;T snv 4
rs11873890
TYMS
18 662135 intron variant A/G snv 8.2E-03 3.2E-02 4
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 4
rs12285095
ZPR1
11 116787315 non coding transcript exon variant T/G snv 9.8E-02 4
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10 4
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 7
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 6
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs13326165
STAB1
3 52498102 intron variant A/G;T snv 3