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Variant (rsID / SNP)

rs576180572

TUBB3

rs576180572 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBB3. Location: chromosome 16, position 90,001,465. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TUBB3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:90001465
Cytoband
16q24.3
HGVS
NM_006086.4(TUBB3):c.606C>T (p.Ile202=)
Allele change
Synonymous_I130I

Public references

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