Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061437
rs1061437
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs10883094
rs10883094
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs11189600
rs11189600
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs17109834
rs17109834
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1739
rs1739
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2296434
rs2296434
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2296435
rs2296435
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2296436
rs2296436
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3750604
rs3750604
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3750605
rs3750605
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3830019
rs3830019
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3830020
rs3830020
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs701801
rs701801
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7921146
rs7921146
Entrez Id: 3257
Gene Symbol: HPS1
HPS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs8181292
rs8181292
Entrez Id: 3257;84795
Gene Symbol: HPS1;PYROXD2
HPS1;PYROXD2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013