Disease: Serum albumin measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs11207997
DOCK7 ; ANGPTL3
1 62596235 intron variant C/T snv 0.39 5
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs1277930
PSRC1
1 109279521 downstream gene variant G/A snv 0.63 4
rs1748197
DOCK7
1 62590441 intron variant G/A snv 0.42 5
rs2131925
DOCK7
1 62560271 intron variant G/T snv 0.57 5
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 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
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 5