Variant (rsID / SNP)

rs35704760

rs35704760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TFR2. Location: chromosome 7, position 100,225,112. Clinical significance in the table: Benign.

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Reference-table entries

TFR2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:100225112
Cytoband: 7q22.1
HGVS: NM_003227.4(TFR2):c.1770C>T (p.Asp590=)
Allele change: Synonymous_D590D

Associated conditions / phenotypes

Hemochromatosis type 3|Hereditary hemochromatosis

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.