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Variant (rsID / SNP)

rs1034489

EPB41L5

rs1034489 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPB41L5. Location: chromosome 2, position 120,885,310. The table records no clinical significance for this variant.

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Reference-table entries

EPB41L5Not classified
Variant type
missense_variant
Chromosome / position
2:120885310
HGVS
NM_020909.4,c.1384G>A,p.Ala462Thr
Allele change
Missense_A462T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.