Variant (rsID / SNP)
rs41291642
rs41291642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3AP1. Location: chromosome 10, position 98,392,816. The table records no clinical significance for this variant.
Reference-table entries
PIK3AP1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 10:98392816
- HGVS
- NM_152309.3,c.1376-4566A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.