DisGeNET - a database of gene-disease associations

Source: ALL

Gene: LINC02169 ×

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

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF _EXOME

AF _GENOME

Disease

Score _vda

EI _vda

N_.PMIDs

FirstRef.

LastRef.

dbSNP:

rs17175620

rs17175620

LINC02169

1.000

0.040

16

54247379

intron variant

G/A

snv

0.13

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs17175655

rs17175655

LINC02169

1.000

0.040

16

54248448

intron variant

C/G;T

snv

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs17254042

rs17254042

LINC02169

1.000

0.040

16

54245491

downstream gene variant

C/G;T

snv

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs17254362

rs17254362

LINC02169

1.000

0.040

16

54255193

intron variant

C/T

snv

0.12

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017

dbSNP:

rs4423418

rs4423418

LINC02169

1.000

0.040

16

54252179

intron variant

A/G

snv

0.23

CUI:	C0023467
Disease:	Leukemia, Myelocytic, Acute

Leukemia, Myelocytic, Acute

0.700

1.000

2017

2017