Variant (rsID / SNP)
rs2240432
rs2240432 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INPP5J. Location: chromosome 22, position 31,521,404. The table records no clinical significance for this variant.
Reference-table entries
INPP5JNot classified
- Variant type
- missense_variant
- Chromosome / position
- 22:31521404
- HGVS
- NM_001284285.2,c.679G>A,p.Ala227Thr
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.