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Variant (rsID / SNP)

rs180798231

ANK3

rs180798231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 61,835,940. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ANK3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:61835940
Cytoband
10q21.2
HGVS
NM_020987.5(ANK3):c.4699G>A (p.Val1567Met)
Allele change
Missense_V1567M

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.