Variant (rsID / SNP)
rs15232
rs15232 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRFIP1. Location: chromosome 2, position 238,671,940. The table records no clinical significance for this variant.
Reference-table entries
LRRFIP1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:238671940
- HGVS
- NM_001137552.2,c.1584C>T,p.Asn528Asn
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
