Variant (rsID / SNP)

rs180801021

rs180801021 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYR. Location: chromosome 11, position 88,961,021. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TYRUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:88961021
Cytoband: 11q14.3
HGVS: NM_000372.5(TYR):c.1067A>T (p.Asp356Val)
Allele change: Missense_D356V

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.