Variant (rsID / SNP)

rs61754362

rs61754362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYR. Location: chromosome 11, position 88,911,734. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

TYRPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:88911734
Cytoband: 11q14.3
HGVS: NM_000372.5(TYR):c.613C>A (p.Pro205Thr)
Allele change: Missense_P205T

Associated conditions / phenotypes

Tyrosinase-negative oculocutaneous albinism

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.