Variant (rsID / SNP)

rs34143170

rs34143170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPHX1. Location: chromosome 1, position 226,027,548. The table records no clinical significance for this variant.

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Reference-table entries

EPHX1Not classified

Variant type: synonymous_variant
Chromosome / position: 1:226027548
HGVS: NM_000120.4,c.741C>T,p.His247His
Allele change: Synonymous_H247H

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.