Variant (rsID / SNP)
rs2277339
rs2277339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRIM1. Location: chromosome 12, position 57,146,069. The table records no clinical significance for this variant.
Reference-table entries
PRIM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:57146069
- HGVS
- NM_000946.3,c.14A>C,p.Asp5Ala
- Allele change
- Missense_D5A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.