DisGeNET - a database of gene-disease associations

SYNE1, spectrin repeat containing nuclear envelope protein 1, 23345

N. diseases: 237; N. variants: 76

Disease: Plexiform leiomyoma ×

Variant: rs58415480 ×

Source: ALL

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:

rs58415480

Entrez Id:	23345
Gene Symbol:	SYNE1

SYNE1

CUI:	C2242776
Disease:

Plexiform leiomyoma

0.700

GeneticVariation

GWASCAT

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.

31649266

2019

dbSNP:

rs58415480

Entrez Id:	23345
Gene Symbol:	SYNE1

SYNE1

CUI:	C2242776
Disease:

Plexiform leiomyoma

0.700

GeneticVariation

GWASCAT

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

31249589

2019

dbSNP:

rs58415480

Entrez Id:	23345
Gene Symbol:	SYNE1

SYNE1

CUI:	C2242776
Disease:

Plexiform leiomyoma

0.700

GeneticVariation

GWASCAT

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.

30194396

2018