Variant (rsID / SNP)

rs10821668

rs10821668 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 61,831,271. Clinical significance in the table: Benign.

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Reference-table entries

ANK3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:61831271
Cytoband: 10q21.2
HGVS: NM_020987.5(ANK3):c.9368A>G (p.Lys3123Arg)
Allele change: Missense_K3123R

Associated conditions / phenotypes

Intellectual disability-hypotonia-spasticity-sleep disorder syndrome

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.