Variant (rsID / SNP)

rs1124777

rs1124777 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3C2B. Location: chromosome 1, position 204,438,334. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PIK3C2BNot classified

Variant type: synonymous_variant
Chromosome / position: 1:204438334
HGVS: NM_001377334.1,c.597G>A,p.Pro199Pro
Allele change: Synonymous_P199P

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.