Variant (rsID / SNP)
rs1048445
rs1048445 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRP12. Location: chromosome 10, position 99,116,903. The table records no clinical significance for this variant.
Reference-table entries
RRP12Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:99116903
- HGVS
- NM_015179.4,c.3842G>A,p.Arg1281Gln
- Allele change
- Missense_R1281Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.