Variant (rsID / SNP)

rs61732397

rs61732397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 61,832,903. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ANK3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:61832903
Cytoband: 10q21.2
HGVS: NM_020987.5(ANK3):c.7736G>A (p.Arg2579Lys)
Allele change: Missense_R2579K

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.