MIR6797

microRNA 6797, the group of MicroRNAs

Basic information

Region (hg38): 19:41869627-41869698

Links

ENSG00000276926NCBI:102465478HGNC:50169GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the MIR6797 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR6797 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 MIR6797

This is a list of pathogenic ClinVar variants found in the MIR6797 region.

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

Position Type Phenotype Significance ClinVar
19-41869682-C-T Diamond-Blackfan anemia Likely benign (Nov 12, 2021)1642265
19-41869689-C-T Diamond-Blackfan anemia Likely benign (Oct 18, 2022)1960938
19-41869693-C-T Diamond-Blackfan anemia Likely benign (Oct 11, 2023)1595351
19-41869694-C-G Diamond-Blackfan anemia 1 Uncertain significance (Jan 13, 2018)894444
19-41869696-C-A Diamond-Blackfan anemia Uncertain significance (Apr 05, 2023)2716436
19-41869697-A-G Diamond-Blackfan anemia Pathogenic (Sep 11, 2023)2736899

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP