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Variant (rsID / SNP)

rs369904982

SPTA1

rs369904982 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTA1. Location: chromosome 1, position 158,621,142. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SPTA1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:158621142
Cytoband
1q23.1
HGVS
NM_003126.4(SPTA1):c.3477+15C>T
Allele change
Silent

Associated conditions / phenotypes

Elliptocytosis 2|Hereditary spherocytosis type 3|Pyropoikilocytosis, hereditary

Public references

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