Variant (rsID / SNP)

rs41303651

rs41303651 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYRP1. Location: chromosome 9, position 12,709,081. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TYRP1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 9:12709081
Cytoband: 9p23
HGVS: NM_000550.3(TYRP1):c.1513C>T (p.Arg505Cys)
Allele change: Missense_R505C

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.