Variant (rsID / SNP)

rs3829925

rs3829925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UCMA. Location: chromosome 10, position 13,275,553. The table records no clinical significance for this variant.

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Reference-table entries

UCMANot classified

Variant type: synonymous_variant
Chromosome / position: 10:13275553
HGVS: NM_145314.3,c.205A>C,p.Arg69Arg
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.