Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs1109748
LOC107984334 ; BEST1
11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs174456
FADS3
11 61888710 intron variant C/A snv 0.59 2
rs174464
FADS3
11 61890454 intron variant A/G snv 0.59 2
rs174468 11 61896219 upstream gene variant G/A snv 0.28 2
rs174472
RAB3IL1
11 61904484 intron variant A/G snv 0.41 2
rs174476
RAB3IL1
11 61906646 synonymous variant C/A;G;T snv 0.30 2
rs174478
RAB3IL1
11 61911104 intron variant T/G snv 0.31 2
rs174479
RAB3IL1
11 61911282 intron variant C/G snv 0.17 2
rs174532
TMEM258 ; MYRF
11 61781402 intron variant G/A snv 0.20 2
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs174579
FADS2
11 61838141 intron variant C/T snv 0.16 2
rs174585
FADS2
11 61844222 intron variant G/A;T snv 2
rs174591
FADS2
11 61850204 intron variant T/A;G snv 2
rs174593
FADS2
11 61851359 intron variant T/C snv 0.24 2
rs174597
FADS2
11 61853568 intron variant G/A;C;T snv 2
rs174605
FADS2
11 61859449 intron variant G/T snv 0.20 2
rs174611
FADS2
11 61860409 intron variant T/C snv 0.21 2
rs174626 11 61869585 downstream gene variant G/A snv 0.48 2