DisGeNET - a database of gene-disease associations

Lacrimoauriculodentodigital syndrome, C0265269

Variant: rs104893886 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs104893886

rs104893886

FGF10

0.800

GeneticVariation

UNIPROT

Mutations in different components of FGF signaling in LADD syndrome.

2006

dbSNP:

rs104893886

rs104893886

FGF10

0.800

GeneticVariation

UNIPROT

LADD syndrome is caused by FGF10 mutations.

2006

dbSNP:

rs104893886

rs104893886

FGF10

C

0.800

CausalMutation

CLINVAR