Variant (rsID / SNP)

rs199850352

rs199850352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 61,822,944. 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: 10:61822944
Cytoband: 10q21.2
HGVS: NM_020987.5(ANK3):c.12520A>G (p.Ile4174Val)
Allele change: Missense_I4174V

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.