Variant (rsID / SNP)

rs301949

rs301949 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPHA6. Location: chromosome 3, position 97,365,074. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

EPHA6Not classified

Variant type: missense_variant
Chromosome / position: 3:97365074
HGVS: NM_001278300.2,c.1072A>G,p.Met358Val
Allele change: Silent

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.