Disease: Serum HDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs11571111
REN
1 204161105 intron variant C/A snv 5.0E-03 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs11635491
LIPC ; ALDH1A2
15 58427542 intron variant G/A snv 0.27 4
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs11873890
TYMS
18 662135 intron variant A/G snv 8.2E-03 3.2E-02 4
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs11960617
SGCD
5 156494033 intron variant C/T snv 1.9E-02 3
rs11999657
IFNB1
9 21078937 upstream gene variant G/A;C snv 3
rs12097137 1 101243889 downstream gene variant G/A;T snv 3
rs12242772
PTEN
10 87944637 intron variant A/G snv 3.0E-02 3
rs12247406
SORCS1
10 106996746 intron variant G/A snv 1.3E-02 3
rs12285095
ZPR1
11 116787315 non coding transcript exon variant T/G snv 9.8E-02 4
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6