DisGeNET - a database of gene-disease associations

rs147257424, MTHFR

N. diseases: 2

Source: ALL

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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.

HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY

CUI:	C1856058
Disease:	HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY

78

0.925

0.080

1

11801299

missense variant

C/A;G;T

snv

1.2E-05; 1.2E-05

0.800

Hepatitis C

CUI:	C0019196
Disease:	Hepatitis C

347

0.925

0.080

1

11801299

missense variant

C/A;G;T

snv

1.2E-05; 1.2E-05

0.010

1.000

2016

2016