Variant (rsID / SNP)

rs41295774

rs41295774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TF. Location: chromosome 3, position 133,476,698. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:133476698
Cytoband: 3q22.1
HGVS: NM_001063.4(TF):c.956A>G (p.His319Arg)
Allele change: Missense_H275R

Associated conditions / phenotypes

Transferrin variant chi|Atransferrinemia

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.