Source: CURATED

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: rs1260326
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 5 2010 2018
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: rs34121855
rs34121855
MLXIPL
7 73626484 upstream gene variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 2 2012 2018
dbSNP: rs780092
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 2 2011 2012
dbSNP: rs11078597
rs11078597
MIR22HG ; WDR81 ; MIR22
17 1715069 intron variant T/C snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs11671010
rs11671010
HPN-AS1
19 35068570 intron variant T/C snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs16948098
rs16948098
FRMD5
15 43927409 intron variant G/A snv 9.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs2293579
rs2293579
PSMC3
11 47419207 intron variant G/A snv 0.35 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs4806073
rs4806073
HPN ; HPN-AS1
19 35064286 intron variant T/C snv 0.85
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs694419
rs694419 		18 62458879 regulatory region variant T/C snv 0.53
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs174548
rs174548
FADS1 ; FADS2
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 3 2008 2013
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: rs102275
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 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: 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: 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: rs174534
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174535
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
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: rs174537
rs174537
MYRF ; TMEM258
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174538
rs174538
TMEM258 ; FEN1 ; MIR611
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013