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Variant (rsID / SNP)

rs775912185

DST

rs775912185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DST. Location: chromosome 6, position 56,507,565. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DSTConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
Deletion
Chromosome / position
6:56507565
Cytoband
6p12.1
HGVS
NM_001723.7(DST):c.22del (p.Tyr8fs)

Associated conditions / phenotypes

Hereditary sensory and autonomic neuropathy type 6|Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.