Variant (rsID / SNP)

rs2071303

rs2071303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HFE. Location: chromosome 6, position 26,091,336. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HFEBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:26091336
Cytoband: 6p22.2
HGVS: NM_000410.4(HFE):c.340+4T>C
Allele change: Silent

Associated conditions / phenotypes

Hereditary hemochromatosis|Hemochromatosis type 1

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.