Variant (rsID / SNP)

rs10009368

rs10009368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PABPC4L. Location: chromosome 4, position 135,121,601. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PABPC4LNot classified

Variant type: missense_variant
Chromosome / position: 4:135121601
HGVS: NM_001114734.2,c.574G>A,p.Val192Ile
Allele change: Missense_V192I

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.