Variant (rsID / SNP)

rs284860

rs284860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WBP1L. Location: chromosome 10, position 104,572,963. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

WBP1LNot classified

Variant type: missense_variant
Chromosome / position: 10:104572963
HGVS: NM_001083913.2,c.967T>C,p.Ser323Pro
Allele change: Missense_S323P

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.