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Variant (rsID / SNP)

rs184910238

TYRP1

rs184910238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYRP1. Location: chromosome 9, position 12,704,582. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TYRP1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:12704582
Cytoband
9p23
HGVS
NM_000550.3(TYRP1):c.1138G>T (p.Ala380Ser)
Allele change
Missense_A380S

Public references

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