Variant (rsID / SNP)

rs3833574

rs3833574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EDAR. Location: chromosome 2, position 109,522,748. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

EDARBenign

Clinical significance (as recorded): Benign
Variant type: Deletion
Chromosome / position: 2:109522748
Cytoband: 2q13
HGVS: NM_022336.4(EDAR):c.1024+16del

Associated conditions / phenotypes

Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant|Autosomal recessive hypohidrotic ectodermal dysplasia syndrome

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.