DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Glioma ×

Variant: rs1217691063 ×

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:

rs1217691063

MTHFR

CUI:	C0017638
Disease:	Glioma

Glioma

0.030

GeneticVariation

BEFREE

No significant differences were found among MTHFR C677T wild type C and variant genotypes CT/TT with glioma patients.

29017962

2018

dbSNP:

rs1217691063

MTHFR

CUI:	C0017638
Disease:	Glioma

Glioma

0.030

GeneticVariation

BEFREE

Association between MTHFR 677C>T polymorphism and risk of gliomas: evidence from a meta-analysis.

23765760

2013

dbSNP:

rs1217691063

MTHFR

CUI:	C0017638
Disease:	Glioma

Glioma

0.030

GeneticVariation

BEFREE

The MTHFR C677T polymorphism seemed to exert no effect on glioma risk.

23846816

2013