Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174478
RAB3IL1
11 61911104 intron variant T/G snv 0.31 2
rs2269928
TMEM258 ; MYRF
11 61770057 intron variant T/G snv 0.18 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2727261
RAB3IL1
11 61944659 regulatory region variant T/C;G snv 2
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174593
FADS2
11 61851359 intron variant T/C snv 0.24 2
rs174602
FADS2
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 3
rs174611
FADS2
11 61860409 intron variant T/C snv 0.21 2
rs17831757
FADS2
11 61867728 downstream gene variant T/C snv 9.3E-02 2
rs422249 11 61872016 downstream gene variant T/C snv 0.67 2
rs4963452 11 62048331 downstream gene variant T/C snv 0.20 2
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 3
rs740006
TMEM258
11 61790396 3 prime UTR variant T/C snv 7.6E-02 2
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs916924
FADS2
11 61851709 intron variant T/C snv 9.1E-02 2
rs174591
FADS2
11 61850204 intron variant T/A;G snv 2
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 3
rs174605
FADS2
11 61859449 intron variant G/T snv 0.20 2