Variant (rsID / SNP)

rs61752939

rs61752939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYRP1. Location: chromosome 9, position 12,698,527. 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: 9:12698527
Cytoband: 9p23
HGVS: NM_000550.3(TYRP1):c.785C>T (p.Thr262Met)
Allele change: Missense_T262M

Associated conditions / phenotypes

Oculocutaneous albinism type 3

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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