DisGeNET - a database of gene-disease associations

FAM222B, family with sequence similarity 222 member B, 55731

N. diseases: 6; N. variants: 33

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:

rs11650788

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C1261502
Disease:

Finding of Mean Corpuscular Hemoglobin

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs9892942

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C0014772
Disease:

Red Blood Cell Count measurement

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs28847895

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C0524587
Disease:

Mean Corpuscular Volume (result)

0.700

GeneticVariation

GWASCAT

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

29403010

2018

dbSNP:

rs12946844

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C1304746
Disease:

RDW - Red blood cell distribution width result

0.700

GeneticVariation

GWASCAT

Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

28957414

2017

dbSNP:

rs12946844

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C0427460
Disease:

Red cell distribution width determination

0.700

GeneticVariation

GWASCAT

Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

28957414

2017

dbSNP:

rs7215310

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C1261502
Disease:

Finding of Mean Corpuscular Hemoglobin

0.700

GeneticVariation

GWASCAT

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.

28017375

2017

dbSNP:

rs35033748

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C1304746
Disease:

RDW - Red blood cell distribution width result

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs35033748

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C0427460
Disease:

Red cell distribution width determination

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs57583458

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

AAAAT

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs9892942

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C1261502
Disease:

Finding of Mean Corpuscular Hemoglobin

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs9892942

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C0524587
Disease:

Mean Corpuscular Volume (result)

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs9914988

Entrez Id:	26284;55731
Gene Symbol:	ERAL1;FAM222B

ERAL1;FAM222B

CUI:	C0206161
Disease:

Reticulocyte count (procedure)

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs1035989

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs11652272

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs11658884

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs12453504

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs17721223

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs2043031

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs2043032

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs2046759

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs4262997

Entrez Id:	55731;100271485
Gene Symbol:	FAM222B;RPL31P58

FAM222B;RPL31P58

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs4794836

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs4795457

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs4795459

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs4795463

Entrez Id:	55731
Gene Symbol:	FAM222B

FAM222B

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012