Variant (rsID / SNP)

rs79284865

rs79284865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HRCT1. Location: chromosome 9, position 35,906,519. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HRCT1Not classified

Variant type: missense_variant
Chromosome / position: 9:35906519
HGVS: NM_001039792.2,c.235G>A,p.Val79Ile
Allele change: Missense_V79I

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.