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Variant (rsID / SNP)

rs5369

EDN1

rs5369 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EDN1. Location: chromosome 6, position 12,294,258. The table records no clinical significance for this variant.

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Reference-table entries

EDN1Not classified
Variant type
synonymous_variant
Chromosome / position
6:12294258
HGVS
NM_001955.5,c.318A>G,p.Glu106Glu
Allele change
Synonymous_E105E

Associated conditions / phenotypes

Ischemia|Pulmonary Edema|Sleep Apnea|Lipid Metabolism Disorder

Public references

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