Variant (rsID / SNP)

rs371525355

rs371525355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP2B3. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ATP2B3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_001001344.3(ATP2B3):c.2434-3C>A
Allele change: Silent

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.