Variant (rsID / SNP)

rs3733082

rs3733082 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTR8. Location: chromosome 3, position 53,914,093. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ACTR8Not classified

Variant type: missense_variant
Chromosome / position: 3:53914093
HGVS: NM_022899.5,c.167C>T,p.Thr56Ile
Allele change: Missense_T56I

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.