Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4775041
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 3 2008 2013
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs108499
rs108499
MYRF ; TMEM258
11 61779765 intron variant C/T snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174455
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174528
rs174528
MYRF ; TMEM258
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174541
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2010 2013
dbSNP: rs174555
rs174555
FADS1 ; FADS2
11 61812288 intron variant T/C snv 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174556
rs174556
FADS1 ; FADS2
0.925 0.160 11 61813163 intron variant C/T snv 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174570
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174576
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174577
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174583
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174611
rs174611
FADS2
11 61860409 intron variant T/C snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174616
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs17821159
rs17821159
ALDH1A2
15 58264863 intron variant A/G snv 0.32
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs2043085
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs2072114
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs2280401
rs2280401
RPS11 ; SNORD35B
19 49496752 intron variant G/A snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 2 2011 2012
dbSNP: rs2524299
rs2524299
FADS2
11 61837310 intron variant A/T snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs261334
rs261334
LIPC ; ALDH1A2 ; LIPC-AS1
15 58434545 intron variant G/C snv 0.73
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
15 58438954 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs2727270
rs2727270
FADS2
11 61835765 intron variant C/T snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs2727271
rs2727271
FADS2
11 61835886 intron variant A/T snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013