MIR3606

microRNA 3606, the group of MicroRNAs

Basic information

Region (hg38): 2:188995630-188995692

Links

ENSG00000284180 ∙ NCBI:100500837 ∙ ∙ HGNC:38881 ∙ ∙ ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the MIR3606 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR3606 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type	Pathogenic	Likely pathogenic	VUS	Likely benign	Benign	Sum
synonymous						0
missense						0
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	0	0	0

Variants in MIR3606

This is a list of pathogenic ClinVar variants found in the MIR3606 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position	Type	Phenotype	Significance	ClinVar
2-188995674-A-G		not specified	Likely benign (Oct 06, 2015)
2-188995675-T-C		Ehlers-Danlos syndrome, type 4	Likely benign (Jan 02, 2024)
2-188995678-C-A		Ehlers-Danlos syndrome, type 4	Likely benign (May 30, 2024)
2-188995680-T-C		Ehlers-Danlos syndrome, type 4	Likely benign (Dec 30, 2023)
2-188995682-C-T		Ehlers-Danlos syndrome, type 4 • Familial thoracic aortic aneurysm and aortic dissection	Likely benign (Jul 22, 2022)
2-188995684-C-A			Uncertain significance (Aug 01, 2016)
2-188995688-T-C		Ehlers-Danlos syndrome, type 4	Likely benign (Dec 13, 2023)
2-188995693-G-T		Ehlers-Danlos syndrome, type 4	Pathogenic (-)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP