Variant (rsID / SNP)

rs2907373

rs2907373 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM20A, PRKAR1A. Location: chromosome 17, position 66,533,655. Clinical significance in the table: Benign.

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Reference-table entries

FAM20ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:66533655
Cytoband: 17q24.2
HGVS: NM_017565.4(FAM20A):c.1589T>C (p.Leu530Ser)
Allele change: Silent

Associated conditions / phenotypes

Amelogenesis imperfecta type 1G

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.