Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 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
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs2338104
KCTD10
1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 3
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87 3
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 4
rs9891572 1.000 0.040 17 2525214 intergenic variant C/T snv 0.17 3
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11