Variant (rsID / SNP)

rs2279199

rs2279199 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UMPS. Location: chromosome 3, position 124,449,252. Clinical significance in the table: Benign.

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Reference-table entries

UMPSBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:124449252
Cytoband: 3q21.2
HGVS: NM_000373.3(UMPS):c.-67T>C
Allele change: Silent

Associated conditions / phenotypes

Orotic aciduria

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.