Variant (rsID / SNP)

rs7923682

rs7923682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 61,828,954. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ANK3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:61828954
Cytoband: 10q21.2
HGVS: NM_020987.5(ANK3):c.11685C>T (p.Ser3895=)
Allele change: Synonymous_S3895S

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.