Disease: Serum HDL cholesterol measurement
Source: GWASDB ×
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
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs7001567
MSRA
8 10257027 intron variant C/G snv 3.7E-02 4
rs5030339
LOC105372272 ; ICAM1
19 10269461 intron variant G/A snv 3.4E-03 5
rs5030361
ICAM1
19 10278833 intron variant C/T snv 6.8E-04 4
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05 4
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs9658292
NOS1
12 117318980 intron variant G/C snv 9.4E-04 5
rs16830551
GSK3B
3 119834031 intron variant C/T snv 2.4E-02 4
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6