Disease: Serum albumin measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
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
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs1277930
PSRC1
1 109279521 downstream gene variant G/A snv 0.63 4
rs17248720
LDLR
19 11087511 upstream gene variant C/T snv 0.16 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
rs2738446
LDLR
19 11116650 intron variant C/A;G snv 0.34 4
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 6
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9