DisGeNET - a database of gene-disease associations

Malformations of Cortical Development, Group II, C1837249

Variant: rs745997770 ×

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:

rs745997770

rs745997770

ASPM

A

0.700

GeneticVariation

CLINVAR

Comprehensive genomic analysis of patients with disorders of cerebral cortical development.

2018