Disease: Serum LDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs9912177
ITGB3
17 47285851 intron variant A/T snv 6.4E-03 3
rs9838771
TGFBR2 ; LOC105377016
3 30657290 intron variant G/A snv 2.5E-02 3
rs9658736
FAS
10 89004160 intron variant T/C snv 9.4E-03 3
rs9658465
NOS1
12 117247093 intron variant T/G snv 2.3E-02 3
rs9658292
NOS1
12 117318980 intron variant G/C snv 9.4E-04 5
rs9658150
PPARD
6 35420123 splice region variant G/A snv 3.6E-05 5.6E-05 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs876528
ADRA1B
5 159964639 intron variant G/A snv 2.3E-02 3
rs8176445
TFPI ; LOC105373786
2 187498080 intron variant T/C snv 8.7E-03 4
rs8138057
PDXP
22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6
rs8105094
HAPLN4
19 19263252 intron variant C/T snv 0.19 4
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs7993724
PDX1 ; PLUT
13 27919139 upstream gene variant T/C snv 5.6E-03 6
rs7951347
CSRP3 ; CSRP3-AS1
11 19198031 intron variant T/A;C snv 3
rs7827408
VPS13B
8 99527615 intron variant C/T snv 2.3E-02 3
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs760242
DHCR7
11 71435530 missense variant C/T snv 2.2E-04 6.3E-05 6
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs734359
EDN2
1 41480231 intron variant C/T snv 7.5E-02 4