Variant (rsID / SNP)

rs61737971

rs61737971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KANK1. Location: chromosome 9, position 710,915. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

KANK1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:710915
Cytoband: 9p24.3
HGVS: NM_015158.5(KANK1):c.149A>T (p.Asp50Val)
Allele change: Missense_D50V

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.