SLC30A6-DT

Chr 2

SLC30A6 divergent transcript

NCBI Gene: 118568811ENSG00000272716
20
ClinVar variants
17
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— SLC30A6-DT
📋
ClinVar Variants
17 Pathogenic / Likely Pathogenic· 2 VUS of 20 total submissions
Some data sources returned errors (1)

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Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

20 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic17
VUS2
Benign1
17
Pathogenic
2
VUS
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————17
Likely Pathogenic
————0
VUS
————2
Likely Benign
————0
Benign
————1
Total—20

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SLC30A6-DT · 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 SLC30A6-DT

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