HCG17

Chr 6

HLA complex group 17

Also known as: LINC00046, NCRNA00046

8
ClinVar variants
6
Pathogenic / LP
pLI score
0
Active trials
Clinical SummaryHCG17
📋
ClinVar Variants
6 Pathogenic / Likely Pathogenic· 2 VUS of 8 total submissions
Some data sources returned errors (1)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/HCG17?content-type=application/json&expand=1

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

8 submitted variants in ClinVar

Classification Summary

Pathogenic5
Likely Pathogenic1
VUS2
5
Pathogenic
1
Likely Pathogenic
2
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
5
Likely Pathogenic
1
VUS
2
Likely Benign
0
Benign
0
Total8

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

HCG17 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

OMIM — Genotype-Phenotype

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →