Variant (rsID / SNP)

rs10852891

rs10852891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPDU1. Location: chromosome 17, position 7,490,810. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MPDU1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:7490810
Cytoband: 17p13.1
HGVS: NM_004870.4(MPDU1):c.685G>A (p.Ala229Thr)
Allele change: Silent

Associated conditions / phenotypes

MPDU1-congenital disorder of glycosylation

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.