DisGeNET - a database of gene-disease associations

ODAPH, odontogenesis associated phosphoprotein, 152816

N. diseases: 6; N. variants: 5

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:

rs146645381

Entrez Id:	152816
Gene Symbol:	ODAPH

ODAPH

CUI:	C3553830
Disease:

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4

0.700

CausalMutation

CLINVAR

dbSNP:

rs1560558455

Entrez Id:	152816
Gene Symbol:	ODAPH

ODAPH

CUI:	C3553830
Disease:

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4

ATGCTGGTTACTGGTA

0.700

CausalMutation

CLINVAR

dbSNP:

rs1560562630

Entrez Id:	152816
Gene Symbol:	ODAPH

ODAPH

CUI:	C3553830
Disease:

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4

0.700

CausalMutation

CLINVAR

dbSNP:

rs1560562738

Entrez Id:	152816
Gene Symbol:	ODAPH

ODAPH

CUI:	C3553830
Disease:

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4

0.700

CausalMutation

CLINVAR

dbSNP:

rs866941536

Entrez Id:	152816
Gene Symbol:	ODAPH

ODAPH

CUI:	C3553830
Disease:

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4

0.700

CausalMutation

CLINVAR