DisGeNET - a database of gene-disease associations

ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT, C4479539

Variant: rs1064797094 ×

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:

rs1064797094

rs1064797094

LGI4

0.800

GeneticVariation

UNIPROT

dbSNP:

rs1064797094

rs1064797094

LGI4

T

0.800

CausalMutation

CLINVAR