DisGeNET - a database of gene-disease associations

Source: GWASCAT

Disease: Leukemia, Myelocytic, Acute ×

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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

Variant

Gene

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF _EXOME

AF _GENOME

Disease

Score _vda

EI _vda

N_.PMIDs

FirstRef.

LastRef.

dbSNP:

rs10222378

rs10222378

FHIT

1.000

0.040

3

61063307

intron variant

A/G;T

snv

0.55

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs13061562

rs13061562

FHIT

1.000

0.040

3

61065916

intron variant

T/C

snv

0.45

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs1965143

rs1965143

FHIT

1.000

0.040

3

61062993

intron variant

T/A;C

snv

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs7642017

rs7642017

FHIT

1.000

0.040

3

61061729

intron variant

C/T

snv

0.61

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs9850713

rs9850713

FHIT

1.000

0.040

3

61062909

intron variant

C/T

snv

0.55

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs9855931

rs9855931

FHIT

1.000

0.040

3

61063887

intron variant

C/G;T

snv

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs9869954

rs9869954

FHIT

1.000

0.040

3

61062586

intron variant

T/A;C

snv

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017