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Variant (rsID / SNP)

rs3747636

PIK3C2B

rs3747636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3C2B. Location: chromosome 1, position 204,403,659. The table records no clinical significance for this variant.

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Reference-table entries

PIK3C2BNot classified
Variant type
synonymous_variant
Chromosome / position
1:204403659
HGVS
NM_001377334.1,c.3594T>C,p.Asn1198Asn
Allele change
Synonymous_N1198N

Public references

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