DisGeNET - a database of gene-disease associations

Child Development Disorders, Pervasive, C0008074

Variant: rs10099100 ×

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:

rs10099100

rs10099100

C

0.700

GeneticVariation

GWASCAT

Identification of common genetic risk variants for autism spectrum disorder.

2019