DisGeNET - a database of gene-disease associations

rs1867503, INHCAP;TF

N. diseases: 1

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

Disease

N. SNPs_d

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF_EXOME

AF_GENOME

Score _vda

EI _vda

N. PMIDs

First Ref.

Last Ref.

Child Development Disorders, Pervasive

CUI:	C0008074
Disease:	Child Development Disorders, Pervasive

379

3

133691804

non coding transcript exon variant

G/A

snv

0.60

0.700

1.000

2015

2015