DisGeNET - a database of gene-disease associations

Variant: rs11614913 ×

Source: ALL

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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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs11614913

HOXC6 ; MIR196A2

0.010

GeneticVariation

BEFREE

The homozygous CC variant and the C allele of the rs11614913</span> (T>C) SNP of miR-196a2 are associated with a significantly reduced risk of ASD.

2016