Variant (rsID / SNP)

rs1805076

rs1805076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP2R1B. Location: chromosome 11, position 111,635,566. Clinical significance in the table: Pathogenic.

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Reference-table entries

PPP2R1BPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:111635566
Cytoband: 11q23.1
HGVS: NM_002716.5(PPP2R1B):c.269G>A (p.Gly90Asp)
Allele change: Missense_G90D

Associated conditions / phenotypes

Lung carcinoma

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.