Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 3
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 3
rs174602
FADS2
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 3
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51 3
rs17764935
RAB3IL1
11 61897285 downstream gene variant G/A snv 4.9E-02 3
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 3
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 3
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs1109748
LOC107984334 ; BEST1
11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs174456
FADS3
11 61888710 intron variant C/A snv 0.59 2