Disease: Serum albumin measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 6
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
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10