Variant (rsID / SNP)

rs145540533

rs145540533 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDSS2. Location: chromosome 6, position 107,475,822. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PDSS2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:107475822
Cytoband: 6q21
HGVS: NM_020381.4(PDSS2):c.*1C>T
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.