Variant (rsID / SNP)

rs61735313

rs61735313 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK1. Location: chromosome 8, position 41,582,031. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ANK1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:41582031
Cytoband: 8p11.21
HGVS: NM_000037.4(ANK1):c.654C>A (p.Asn218Lys)
Allele change: Missense_N218K

Associated conditions / phenotypes

Hereditary spherocytosis type 1|Spherocytosis

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.