Disease: High density lipoprotein measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
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
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv 4
rs11652146
ZNF652
17 49345001 intron variant G/A;C snv 4
rs11765979
LOC105375508
7 130761118 intergenic variant A/C;G snv 2
rs11856159
ALDH1A2
15 58406811 intron variant C/A;G;T snv 4
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 5
rs11987974
LOC105379376
8 36966299 intergenic variant C/A;T snv 4
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 4
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs13326165
STAB1
3 52498102 intron variant A/G;T snv 3
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 3
rs148149124
TUBGCP4
15 43382233 intron variant TAAAAGAAAAA/-;TAAAAGAAAAATAAAAGAAAAA delins 2
rs149580368 17 43797377 downstream gene variant C/A snv 2
rs150090666
PDE3B
11 14843853 stop gained C/G;T snv 8.0E-06; 5.8E-04 2
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 12
rs1558861 11 116736721 regulatory region variant C/G;T snv 5