TARID

Chr 6

TCF21 antisense RNA inducing promoter demethylation

NCBI Gene: 100507308ENSG00000227954
470
ClinVar variants
28
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— TARID
📋
ClinVar Variants
28 Pathogenic / Likely Pathogenic· 254 VUS of 470 total submissions
Some data sources returned errors (1)

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

470 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic18
Likely Pathogenic10
VUS254
Likely Benign139
Benign31
Conflicting18
18
Pathogenic
10
Likely Pathogenic
254
VUS
139
Likely Benign
31
Benign
18
Conflicting

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
7
1
10
0
18
Likely Pathogenic
6
0
4
0
10
VUS
6
185
61
2
254
Likely Benign
0
0
59
80
139
Benign
0
0
31
0
31
Conflicting
—18
Total1918616582470

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

TARID · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC
Top 5 resultsSearch Europe PMC ↗

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools