DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Cryptorchidism ×

Variant: rs121912555 ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs121912555

INSL3

CUI:	C0010417
Disease:	Cryptorchidism

Cryptorchidism

0.800

GeneticVariation

UNIPROT

A novel mutation of the insulin-like 3 gene in patients with cryptorchidism.

12601553

2003

dbSNP:

rs121912555

INSL3

CUI:	C0010417
Disease:	Cryptorchidism

Cryptorchidism

0.800

GeneticVariation

UNIPROT

Novel insulin-like 3 (INSL3) gene mutation associated with human cryptorchidism.

11746019

2001

dbSNP:

rs121912555

INSL3

CUI:	C0010417
Disease:	Cryptorchidism

Cryptorchidism

0.800

GeneticVariation

UNIPROT

Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism.

11095425

2000

dbSNP:

rs121912555

INSL3

CUI:	C0010417
Disease:	Cryptorchidism

Cryptorchidism

0.800

CausalMutation

CLINVAR