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Variant (rsID / SNP)

rs1553921

PIK3C2B

rs1553921 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3C2B. Location: chromosome 1, position 204,438,643. The table records no clinical significance for this variant.

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Reference-table entries

PIK3C2BNot classified
Variant type
synonymous_variant
Chromosome / position
1:204438643
HGVS
NM_001377334.1,c.288C>A,p.Leu96Leu
Allele change
Synonymous_L96L

Public references

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