Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs174579
FADS2
11 61838141 intron variant C/T snv 0.16 2
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs2727270
FADS2
11 61835765 intron variant C/T snv 0.12 2
rs412334
FEN1 ; TMEM258 ; MIR611
11 61792789 5 prime UTR variant C/T snv 0.10 2
rs650436
TMEM258 ; MYRF
11 61768958 intron variant C/T snv 0.39 2
rs7935946
FADS2
11 61848070 5 prime UTR variant C/T snv 0.11 2
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs174468 11 61896219 upstream gene variant G/A snv 0.28 2
rs174532
TMEM258 ; MYRF
11 61781402 intron variant G/A snv 0.20 2
rs174538
TMEM258 ; MIR611 ; FEN1
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51 3
rs174626 11 61869585 downstream gene variant G/A snv 0.48 2
rs17762402
TMEM258 ; MYRF
11 61785729 intron variant G/A snv 4.8E-02 2
rs17764935
RAB3IL1
11 61897285 downstream gene variant G/A snv 4.9E-02 3
rs2526678
FADS2
11 61856321 non coding transcript exon variant G/A snv 8.6E-02 2
rs579383
MYRF ; TMEM258
11 61769111 intron variant G/A snv 0.58 2