Variant (rsID / SNP)

rs115020236

rs115020236 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KANK1. Location: chromosome 9, position 712,567. Clinical significance in the table: Likely benign.

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Reference-table entries

KANK1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:712567
Cytoband: 9p24.3
HGVS: NM_015158.5(KANK1):c.1801G>A (p.Glu601Lys)
Allele change: Missense_E601K

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.