DisGeNET - a database of gene-disease associations

Childhood Neuroblastoma, C4086165

Variant: rs2168101 ×

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:

rs2168101

LMO1 ; LOC105376536

0.030

GeneticVariation

BEFREE

Our findings revealed that rs110419 and rs2168101 polymorphisms were significantly associated with a decreased risk of NB in all genetic models.

31830377

2020

dbSNP:

rs2168101

LMO1 ; LOC105376536

0.030

GeneticVariation

BEFREE

<b>Results:</b> Significant associations with neuroblastoma risk were found for four (rs110419, rs4758051, rs10840002, and rs2168101) out of the five polymorphisms.

30406033

2018

dbSNP:

rs2168101

LMO1 ; LOC105376536

0.030

GeneticVariation

BEFREE

In summary, the current study confirmed that the potentially functional <i>LMO1</i> rs2168101 G>T and rs3750952 G>C polymorphisms were associated with neuroblastoma susceptibility.

29760797

2018