Disease: Serum albumin measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
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
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs1277930
PSRC1
1 109279521 downstream gene variant G/A snv 0.63 4
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs17248720
LDLR
19 11087511 upstream gene variant C/T snv 0.16 4
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 6
rs2738446
LDLR
19 11116650 intron variant C/A;G snv 0.34 4
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 5
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6