Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9924951
RBFOX1
16 7454852 intron variant G/A snv 0.39 2
rs4963452 11 62048331 downstream gene variant T/C snv 0.20 2
rs1109748
LOC107984334 ; BEST1
11 61955173 synonymous variant C/A snv 0.21 0.11 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
rs2521568
RAB3IL1
11 61933461 upstream gene variant G/C snv 9.5E-02 2
rs174479
RAB3IL1
11 61911282 intron variant C/G snv 0.17 2
rs174478
RAB3IL1
11 61911104 intron variant T/G snv 0.31 2
rs174476
RAB3IL1
11 61906646 synonymous variant C/A;G;T snv 0.30 2
rs174472
RAB3IL1
11 61904484 intron variant A/G snv 0.41 2
rs17764935
RAB3IL1
11 61897285 downstream gene variant G/A snv 4.9E-02 3
rs174468 11 61896219 upstream gene variant G/A snv 0.28 2
rs174464
FADS3
11 61890454 intron variant A/G snv 0.59 2
rs174456
FADS3
11 61888710 intron variant C/A snv 0.59 2
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs7394871
FADS3
11 61885042 intron variant A/C;T snv 2
rs174634
MIR6746 ; FADS3
11 61879915 intron variant G/C;T snv 2
rs7942717
MIR6746 ; FADS3
11 61879816 intron variant G/A snv 0.89 2
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 3
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs7482316 11 61872726 downstream gene variant G/A;C snv 2
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs422249 11 61872016 downstream gene variant T/C snv 0.67 2
rs7104849 11 61870572 downstream gene variant G/A;T snv 2