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Variant (rsID / SNP)

rs1051741

EPHX1

rs1051741 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPHX1. Location: chromosome 1, position 226,032,229. The table records no clinical significance for this variant.

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Reference-table entries

EPHX1Not classified
Variant type
synonymous_variant
Chromosome / position
1:226032229
HGVS
NM_000120.4,c.1071C>T,p.Asn357Asn
Allele change
Synonymous_N357N

Associated conditions / phenotypes

Occupational Asthma

Public references

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