Variant (rsID / SNP)

rs200234622

rs200234622 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KNL1. Location: chromosome 15, position 40,898,604. Clinical significance in the table: Uncertain significance.

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Reference-table entries

KNL1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:40898604
Cytoband: 15q15.1
HGVS: NM_144508.5(KNL1):c.89C>T (p.Pro30Leu)
Allele change: Missense_P30L

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.