DisGeNET - a database of gene-disease associations

Autistic Disorder, C0004352

Variant: rs7180500 ×

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:

rs7180500

rs7180500

GABRG3

0.010

GeneticVariation

BEFREE

Our results showed that the C allele of rs7180500 in GABRG3 was a risk variant for autism (p = 0.00057).

2018