Disease: High density lipoprotein measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs5742626
LINC02456 ; IGF1
12 102464131 intron variant T/C snv 2.3E-02 3
rs2075847
WTAPP1 ; MMP1
11 102799093 intron variant A/C;G snv 3
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs11824953
MMP13
11 102949239 intron variant C/G snv 2.7E-02 3
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs34400162
GSTO2
10 104275312 missense variant G/A snv 5.6E-04 1.7E-03 3
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 6
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs4455790
RP1L1
8 10634174 intron variant C/G snv 0.74 2
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs752273 2 108314649 upstream gene variant T/A snv 0.23 2
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs41278045
PLA2G12A
4 109717608 missense variant A/G snv 5.6E-04 8.9E-04 2
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs7998875
COL4A1
13 110289053 intron variant G/A;T snv 3
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4