DisGeNET - a database of gene-disease associations

Source: CLINVAR

Disease: Leukemia, Myelocytic, Acute ×

Gene: SF3B1 ×

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:

rs1057519755

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs1057519755

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs1057519756

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs1057519756

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs1057519756

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs374250186

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.

23634996

2013

dbSNP:

rs374250186

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.

23634996

2013

dbSNP:

rs377023736

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs377023736

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs559063155

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs559063155

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs559063155

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia.

23395771

2013

dbSNP:

rs754688962

SF3B1

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

CLINVAR

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.

23634996

2013