Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4
rs10402729
NCAN
19 19244291 intron variant T/C snv 3.3E-02 4
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02 4
rs11568767
TGFBR1
9 99132990 intron variant C/T snv 3.7E-03 4
rs11574980
CPB2-AS1 ; CPB2
13 46105177 non coding transcript exon variant T/C snv 2.1E-02 4
rs12394306
SYN1
X 47576648 splice region variant A/C;T snv 4.3E-03 4
rs16830551
GSK3B
3 119834031 intron variant C/T snv 2.4E-02 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05 4
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 4
rs5030361
ICAM1
19 10278833 intron variant C/T snv 6.8E-04 4
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 4
rs7001567
MSRA
8 10257027 intron variant C/G snv 3.7E-02 4
rs7218945
NCOR1
17 16133280 intron variant A/G snv 2.5E-02 4
rs7925853
SOX6
11 16374856 intron variant A/T snv 4.8E-02 4
rs8006570
CHURC1-FNTB ; RAB15
14 64945992 3 prime UTR variant G/A snv 5.4E-02 4
rs9341059
ESR1
6 152097101 intron variant C/A;T snv 4
rs9465848
CDKAL1
6 20635589 intron variant C/T snv 9.3E-03 4
rs9913758
MYOCD ; LOC100128006
17 12763404 synonymous variant C/G;T snv 6.5E-03; 4.1E-06 2.6E-02 4
rs9913813
LOC105371790
17 44277325 intron variant G/A snv 1.9E-02 4
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5