Variant (rsID / SNP)

rs114076603

rs114076603 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KANK1. Location: chromosome 9, position 711,399. 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: 9:711399
Cytoband: 9p24.3
HGVS: NM_015158.5(KANK1):c.633G>C (p.Gln211His)
Allele change: Missense_Q211H

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.