Variant (rsID / SNP)

rs35668691

rs35668691 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3AP1. Location: chromosome 10, position 98,411,293. Clinical significance in the table: Benign.

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Reference-table entries

PIK3AP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:98411293
Cytoband: 10q24.1
HGVS: NM_152309.3(PIK3AP1):c.828C>T (p.Ala276=)
Allele change: Synonymous_A276A

Associated conditions / phenotypes

Infantile spasms

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.