Variant (rsID / SNP)

rs148904927

rs148904927 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 61,833,414. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ANK3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:61833414
Cytoband: 10q21.2
HGVS: NM_020987.5(ANK3):c.7225T>C (p.Ser2409Pro)
Allele change: Missense_S2409P

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.