Variant (rsID / SNP)

rs147404722

rs147404722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPRN. Location: chromosome 9, position 140,094,273. Clinical significance in the table: Benign.

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Reference-table entries

TPRNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:140094273
Cytoband: 9q34.3
HGVS: NM_001128228.3(TPRN):c.891C>G (p.Phe297Leu)
Allele change: Missense_F297L

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.