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Variant (rsID / SNP)

rs1052878

ELAPOR1

rs1052878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ELAPOR1. Location: chromosome 1, position 109,745,618. The table records no clinical significance for this variant.

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Reference-table entries

ELAPOR1Not classified
Variant type
missense_variant
Chromosome / position
1:109745618
HGVS
NM_020775.5,c.3026T>C,p.Leu1009Pro
Allele change
Silent

Public references

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