MIR6752

microRNA 6752, the group of MicroRNAs

Basic information

Region (hg38): 11:67490245-67490315

Links

ENSG00000276769NCBI:102465450HGNC:50020GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the MIR6752 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR6752 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 MIR6752

This is a list of pathogenic ClinVar variants found in the MIR6752 region.

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

Position Type Phenotype Significance ClinVar
11-67490296-C-G Benign (Oct 15, 2024)1585349
11-67490298-C-T Likely benign (Nov 10, 2022)1429633
11-67490301-C-T Likely benign (Aug 11, 2024)3682454
11-67490302-C-T Likely benign (Aug 14, 2024)1581829
11-67490304-C-T Likely benign (Jul 10, 2023)1566651
11-67490306-A-G Likely benign (Sep 18, 2024)1643181
11-67490306-A-T Likely benign (Nov 15, 2020)1652039
11-67490312-C-T Likely benign (Jun 04, 2024)1930944
11-67490313-C-T Hereditary cancer-predisposing syndrome Uncertain significance (Feb 15, 2024)1362636
11-67490316-G-T Somatotroph adenoma not provided (-)41193

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP