Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434439
rs121434439
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.800 GeneticVariation UNIPROT Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3. 21990100 2012
dbSNP: rs121434440
rs121434440
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.800 GeneticVariation UNIPROT Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3. 21990100 2012
dbSNP: rs121434439
rs121434439
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.800 GeneticVariation UNIPROT Impaired membrane traffic in defective ether lipid biosynthesis. 11152660 2001
dbSNP: rs121434440
rs121434440
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.800 GeneticVariation UNIPROT Impaired membrane traffic in defective ether lipid biosynthesis. 11152660 2001
dbSNP: rs121434439
rs121434439
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.800 GeneticVariation UNIPROT Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2. 9536089 1998
dbSNP: rs121434440
rs121434440
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.800 GeneticVariation UNIPROT Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2. 9536089 1998
dbSNP: rs121434439
rs121434439
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
A 0.800 CausalMutation CLINVAR
dbSNP: rs121434440
rs121434440
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.700 GeneticVariation UNIPROT Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3. 21990100 2012
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.700 GeneticVariation UNIPROT Impaired membrane traffic in defective ether lipid biosynthesis. 11152660 2001
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C1857242
Disease:
Rhizomelic chondrodysplasia punctata, type 2
0.700 GeneticVariation UNIPROT Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2. 9536089 1998
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C3469186
Disease:
HEMOCHROMATOSIS, TYPE 1
0.020 GeneticVariation BEFREE  GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis. 27740525 2017
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C3469186
Disease:
HEMOCHROMATOSIS, TYPE 1
0.020 GeneticVariation BEFREE GNPAT rs11558492 minor allele (G) frequency (MAF) was 20.3% in HFE-HH, 17.2% in controls and 20.6% in EVS database. 28425416 2017
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C0282193
Disease:
Iron Overload
0.020 GeneticVariation BEFREE Previous studies in high and low expressors has demonstrated that a variant in the GNPAT gene (D519G, Rs11558492, chromosome 1, exon 11) has been associated with severe iron overload in C282Y homozygotes for hemochromatosis. 27740525 2017
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C0018995
Disease:
Hemochromatosis
0.020 GeneticVariation BEFREE GNPAT rs11558492 minor allele (G) frequency (MAF) was 20.3% in HFE-HH, 17.2% in controls and 20.6% in EVS database. 28425416 2017
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C0018995
Disease:
Hemochromatosis
0.020 GeneticVariation BEFREE  GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis. 27740525 2017
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C0282193
Disease:
Iron Overload
0.020 GeneticVariation BEFREE Sixteen of twenty-two participants with severe iron overload had glyceronephosphate O-acyltransferase (GNPAT) polymorphism p.D519G (rs11558492; 15 heterozygotes, one homozygote). 25605615 2015
dbSNP: rs11558492
rs11558492
Entrez Id: 8443
Gene Symbol: GNPAT
GNPAT
CUI: C0239946
Disease:
Fibrosis, Liver
0.010 GeneticVariation BEFREE Our findings indicate that GNPAT rs11558492 is not a major modifier of iron status and is not associated with liver fibrosis in HFE-HH patients. 28425416 2017