Variant (rsID / SNP)

rs301948

rs301948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPHA6. Location: chromosome 3, position 97,365,038. The table records no clinical significance for this variant.

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Reference-table entries

EPHA6Not classified

Variant type: missense_variant
Chromosome / position: 3:97365038
HGVS: NM_001278300.2,c.1036G>A,p.Glu346Lys
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.