FAM88B

Chr 9

family with sequence similarity 88 member B

NCBI Gene: 728673ENSG00000170161
21
ClinVar variants
0
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— FAM88B
📋
ClinVar Variants
21 total variants — no pathogenic classifications of 21 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

21 submitted variants in ClinVar

ClinVar

Classification Summary

Protein Context — Lollipop Plot

FAM88B · 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

No publications found for FAM88B

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