Variant (rsID / SNP)

rs41296598

rs41296598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TF. Location: chromosome 3, position 133,494,394. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TFUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 3:133494394
Cytoband: 3q22.1
HGVS: NM_001063.4(TF):c.1805C>A (p.Pro602Gln)
Allele change: Missense_P558L

Associated conditions / phenotypes

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.