Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 3
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs174538
TMEM258 ; MIR611 ; FEN1
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs174476
RAB3IL1
11 61906646 synonymous variant C/A;G;T snv 0.30 2
rs1109748
LOC107984334 ; BEST1
11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
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
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
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
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 3
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5