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: 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: rs174449
rs174449 		11 61872907 downstream gene variant G/A snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174536
rs174536
MYRF ; TMEM258
11 61784455 non coding transcript exon variant A/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 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: 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: 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: 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: rs2286963
rs2286963
ACADL
2 210195326 missense variant T/G snv 0.30 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2010 2013
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
dbSNP: rs7072216
rs7072216
PYROXD2 ; MIR1287
10 98397096 intron variant T/C snv 0.51
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2011 2013
dbSNP: rs10007186
rs10007186
LINC01094
4 78667891 intron variant C/T snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1001159
rs1001159 		9 36728588 intergenic variant C/T snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10018448
rs10018448
PPM1K-DT
4 88304019 intron variant A/G snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10024717
rs10024717
PPM1K-DT
4 88298493 intron variant G/A snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1002475
rs1002475
REV3L ; MFSD4B
6 111388386 intron variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1002687
rs1002687
DOCK7
1 62498066 intron variant G/A snv 0.57
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10057473
rs10057473 		5 143507813 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1007205
rs1007205
DOCK7
1 62471241 intron variant T/A;C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1007995
rs1007995
LOC101927502
9 81757012 intron variant A/G snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10095723
rs10095723
LOXL2 ; ENTPD4
8 23385810 3 prime UTR variant T/C snv 8.0E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10096495
rs10096495
LOXL2 ; ENTPD4
8 23388270 intron variant C/T snv 8.7E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013