Variant (rsID / SNP)

rs200599944

rs200599944 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM20A, PRKAR1A. Location: chromosome 17, position 66,536,033. Clinical significance in the table: Uncertain significance.

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Reference-table entries

FAM20AUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:66536033
Cytoband: 17q24.2
HGVS: NM_017565.4(FAM20A):c.1294G>A (p.Ala432Thr)
Allele change: Silent

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.