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
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02 4
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11568767
TGFBR1
9 99132990 intron variant C/T snv 3.7E-03 4
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs11574980
CPB2-AS1 ; CPB2
13 46105177 non coding transcript exon variant T/C snv 2.1E-02 4
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs12394306
SYN1
X 47576648 splice region variant A/C;T snv 4.3E-03 4
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
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
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs17243641
LOC105376326 ; TRAF2 ; MIR4479
9 136886986 intron variant G/T snv 2.6E-03 5
rs17404153
DNAJC13
3 132444356 intron variant G/T snv 0.10 5