DisGeNET - a database of gene-disease associations

Conotruncal defect, C1853238

Variant: rs4705343 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs4705343

rs4705343

MIR143 ; CARMN

0.010

GeneticVariation

BEFREE

<b>Results:</b> An association between SNP rs4705343</span> of <i>miR-143/145</i> and CTDs has been confirmed in the Chinese Han population.

2019