Variant (rsID / SNP)

rs28763991

rs28763991 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIK3CG. Location: chromosome 7, position 106,522,592. The table records no clinical significance for this variant.

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Reference-table entries

PIK3CGNot classified

Variant type: missense_variant
Chromosome / position: 7:106522592
HGVS: NM_001282426.2,c.2569A>G,p.Thr857Ala
Allele change: Missense_T857A

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.