Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17762402
TMEM258 ; MYRF
11 61785729 intron variant G/A snv 4.8E-02 2
rs17764324
FADS2
11 61867616 downstream gene variant G/A;T snv 2
rs17831757
FADS2
11 61867728 downstream gene variant T/C snv 9.3E-02 2
rs2269928
TMEM258 ; MYRF
11 61770057 intron variant T/G snv 0.18 2
rs2521568
RAB3IL1
11 61933461 upstream gene variant G/C snv 9.5E-02 2
rs2524299
FADS2
11 61837310 intron variant A/T snv 0.17 2
rs2526678
FADS2
11 61856321 non coding transcript exon variant G/A snv 8.6E-02 2
rs2727261
RAB3IL1
11 61944659 regulatory region variant T/C;G snv 2
rs2727266
RAB3IL1
11 61936862 upstream gene variant A/G snv 9.8E-02 2
rs2727270
FADS2
11 61835765 intron variant C/T snv 0.12 2
rs2727271
FADS2
11 61835886 intron variant A/T snv 0.12 2
rs412334
FEN1 ; TMEM258 ; MIR611
11 61792789 5 prime UTR variant C/T snv 0.10 2
rs422249 11 61872016 downstream gene variant T/C snv 0.67 2
rs4453795
FGF12
3 192376186 intron variant A/G;T snv 2
rs4963452 11 62048331 downstream gene variant T/C snv 0.20 2
rs579383
MYRF ; TMEM258
11 61769111 intron variant G/A snv 0.58 2
rs650436
TMEM258 ; MYRF
11 61768958 intron variant C/T snv 0.39 2
rs7104849 11 61870572 downstream gene variant G/A;T snv 2
rs7394871
FADS3
11 61885042 intron variant A/C;T snv 2
rs740006
TMEM258
11 61790396 3 prime UTR variant T/C snv 7.6E-02 2
rs7482316 11 61872726 downstream gene variant G/A;C snv 2
rs7935946
FADS2
11 61848070 5 prime UTR variant C/T snv 0.11 2
rs7942717
MIR6746 ; FADS3
11 61879816 intron variant G/A snv 0.89 2
rs916924
FADS2
11 61851709 intron variant T/C snv 9.1E-02 2
rs9924951
RBFOX1
16 7454852 intron variant G/A snv 0.39 2