SLC30A6-DT

Chr 2

SLC30A6 divergent transcript

I cannot provide a clinical gene summary for SLC30A6-DT because no functional, phenotypic, or inheritance information was provided in the data. SLC30A6-DT appears to be a non-coding RNA transcript associated with the SLC30A6 gene region, but without specific information about its role or associated diseases, I cannot make clinically relevant statements about this gene.

Research

ResearchGenerating clinical summary…

Clinical Summary— SLC30A6-DT

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ClinVar Variants

9 unique Pathogenic / Likely Pathogenic of 9 total submissions

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Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

9 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic9

Pathogenic

Curated Variants Distribution

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

Classification	LoF	Missense + Inframe	Non-coding	Synonymous	Total
Pathogenic	—	—	—	—	9
Likely Pathogenic	—	—	—	—	0
VUS	—	—	—	—	0
Likely Benign	—	—	—	—	0
Benign	—	—	—	—	0
Total	—				9

Counts from ClinVar esearch · Updated hourly

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8 pathogenic / likely-pathogenic (of 11) ClinVar copy-number / structural variants overlap SLC30A6-DT — these span large chromosomal regions, not the gene specifically, and are excluded from the counts above. Explore in CNV tools →