DisGeNET - a database of gene-disease associations

HYDIN, HYDIN axonemal central pair apparatus protein, 54768

N. diseases: 61; N. variants: 7

Disease: Ciliary Dyskinesia, Primary, 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:

rs373501414

rs373501414

Entrez Id:	54768
Gene Symbol:	HYDIN

HYDIN

CUI:	C1837615
Disease:

Ciliary Dyskinesia, Primary, 5

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs397515413

rs397515413

Entrez Id:	54768
Gene Symbol:	HYDIN

HYDIN

CUI:	C1837615
Disease:

Ciliary Dyskinesia, Primary, 5

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs397515414

rs397515414

Entrez Id:	54768
Gene Symbol:	HYDIN

HYDIN

CUI:	C1837615
Disease:

Ciliary Dyskinesia, Primary, 5

A

0.700

CausalMutation

CLINVAR