Variant (rsID / SNP)

rs3818562

rs3818562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPS8L3. Location: chromosome 1, position 110,300,441. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

EPS8L3Not classified

Variant type: missense_variant
Chromosome / position: 1:110300441
HGVS: NM_139053.3,c.880C>T,p.His294Tyr
Allele change: Missense_H260Y

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.