Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs4453795
FGF12
3 192376186 intron variant A/G;T snv 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs650436
TMEM258 ; MYRF
11 61768958 intron variant C/T snv 0.39 2
rs579383
MYRF ; TMEM258
11 61769111 intron variant G/A snv 0.58 2
rs2269928
TMEM258 ; MYRF
11 61770057 intron variant T/G snv 0.18 2
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 3
rs174532
TMEM258 ; MYRF
11 61781402 intron variant G/A snv 0.20 2
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs17762402
TMEM258 ; MYRF
11 61785729 intron variant G/A snv 4.8E-02 2
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18