DisGeNET - a database of gene-disease associations

Autistic Disorder, C0004352

Variant: rs1800562 ×

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:

rs1800562

rs1800562

HFE ; LOC108783645

0.010

GeneticVariation

BEFREE

No significant association of p.H63D nor p</span>.C282Y polymorphism and autism was revealed.

2011