DisGeNET - a database of gene-disease associations

PYROXD2, pyridine nucleotide-disulphide oxidoreductase domain 2, 84795

N. diseases: 12; N. variants: 86

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs17109605

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs17109634

Entrez Id:	84795;100302133
Gene Symbol:	PYROXD2;MIR1287

PYROXD2;MIR1287

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs2147897

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs2274248

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs2274249

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs4345897

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs4400721

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs701801

Entrez Id:	3257;84795
Gene Symbol:	HPS1;PYROXD2

HPS1;PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs701801

Entrez Id:	3257;84795
Gene Symbol:	HPS1;PYROXD2

HPS1;PYROXD2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

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:

rs10748729

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10786415

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10786418

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10883084

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10883085

Entrez Id:	84795;100302133
Gene Symbol:	PYROXD2;MIR1287

PYROXD2;MIR1287

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10883087

Entrez Id:	84795;100302133
Gene Symbol:	PYROXD2;MIR1287

PYROXD2;MIR1287

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10883089

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs10883092

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs11189586

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs11189590

Entrez Id:	84795;100302133
Gene Symbol:	PYROXD2;MIR1287

PYROXD2;MIR1287

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs11189592

Entrez Id:	84795;100302133
Gene Symbol:	PYROXD2;MIR1287

PYROXD2;MIR1287

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs11597425

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs11597428

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs12763326

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs12763379

Entrez Id:	84795
Gene Symbol:	PYROXD2

PYROXD2

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013