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
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
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
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
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 6
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 5
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
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
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs17248720
LDLR
19 11087511 upstream gene variant C/T snv 0.16 4
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 4
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
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
rs1748197
DOCK7
1 62590441 intron variant G/A snv 0.42 5