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Variant (rsID / SNP)

rs2271420

PIK3C2B

rs2271420 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3C2B. Location: chromosome 1, position 204,399,064. The table records no clinical significance for this variant.

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Reference-table entries

PIK3C2BNot classified
Variant type
synonymous_variant
Chromosome / position
1:204399064
HGVS
NM_001377334.1,c.4383C>T,p.Pro1461Pro
Allele change
Synonymous_P1461P

Associated conditions / phenotypes

Depression

Public references

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