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: rs3733402
rs3733402
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2014
dbSNP: rs11132382
rs11132382
4 186222648 intron variant T/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs13136536
rs13136536
4 186217309 intron variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs1511801
rs1511801
4 186229556 intron variant A/T snv 0.59
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs1912826
rs1912826
4 186228386 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs1912826
rs1912826
4 186228386 intron variant G/A;C snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs2048
rs2048
4 186226979 intron variant G/T snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2102575
rs2102575
4 186210350 intron variant G/A snv 0.90
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2012 2012
dbSNP: rs2304595
rs2304595
1.000 0.040 4 186251126 non coding transcript exon variant G/A snv 0.36
Activated Partial Thromboplastin Time measurement
0.700 1.000 1 2013 2013
dbSNP: rs28671360
rs28671360
4 186257634 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs3087505
rs3087505
4 186258332 3 prime UTR variant A/G snv 0.91
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2012 2012
dbSNP: rs33930717
rs33930717
4 186257634 intron variant -/TGT;TTT delins
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs35328399
rs35328399
4 186217309 intron variant -/GTT delins
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs35984397
rs35984397
4 186240347 intron variant G/A snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs3733402
rs3733402
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs3775298
rs3775298
4 186229324 intron variant A/G snv 0.59
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4241815
rs4241815
4 186230988 intron variant C/T snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4241816
rs4241816
4 186231173 intron variant A/T snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4241817
rs4241817
4 186231504 intron variant T/C snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4241818
rs4241818
4 186232632 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4253236
rs4253236
4 186226917 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4253238
rs4253238
0.925 0.080 4 186227233 intron variant C/T snv 0.59
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4253238
rs4253238
0.925 0.080 4 186227233 intron variant C/T snv 0.59
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs4253244
rs4253244
4 186232621 intron variant C/A snv 0.70
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4253248
rs4253248
4 186234334 intron variant G/A snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012