FAM66B

Chr 8

family with sequence similarity 66 member B

Also known as: FAM66E

0
Active trials
37
Pathogenic / LP
107
ClinVar variants
0
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryFAM66B
📋
ClinVar Variants
37 Pathogenic / Likely Pathogenic of 107 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

107 submitted variants in ClinVar

Classification Summary

Pathogenic37
Likely Benign6
Benign64
37
Pathogenic
6
Likely Benign
64
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
37
Likely Pathogenic
0
VUS
0
Likely Benign
6
Benign
64
Total107

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

FAM66B · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found