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
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 6
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 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
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 4
rs17248720
LDLR
19 11087511 upstream gene variant C/T snv 0.16 4
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 4
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs2738446
LDLR
19 11116650 intron variant C/A;G snv 0.34 4