{{Rsnum
|rsid=1805076
|Gene=PPP2R1B
|Chromosome=11
|position=111764842
|Orientation=plus
|GMAF=0.007346
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PPP2R1B
}}{{omim
|id=603113
|rsnum=1805076
|variant=0001
}}{{ClinVar
|rsid=1805076
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=111635566
|CHROM=11
|GMAF=0.0073
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x05026000000004051e110100
|GENEINFO=PPP2R1B:5519
|GENE_NAME=PPP2R1B
|GENE_ID=5519
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.111635566C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;VLD;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CAF=0.9927; 0.007346
|CLNACC=RCV000007000.1
|CLNDBN=Lung cancer
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1108:C0684249:211980:187875007
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603113.0001
|COMMON=1
|Disease=Lung cancer
}}{{GET Evidence
|gene=PPP2R1B
|aa_change=Gly90Asp
|aa_change_short=G90D
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=dominant
|quality_scores=Array
|dbsnp_id=rs1805076
|overall_frequency_n=86
|overall_frequency_d=10758
|overall_frequency=0.00799405
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=2
|n_articles_annotated=2
|qualityscore_in_silico=1
|qualitycomment_in_silico=Y
|qualityscore_in_vitro=1
|qualitycomment_in_vitro=Y
|qualityscore_case_control=2
|qualitycomment_case_control=Y
|qualityscore_familial=1
|qualitycomment_familial=Y
|qualityscore_severity=3
|in_omim=Y
|nblosum100=4
|autoscore=3
|webscore=N
|summary_short=Associated with increased incidence of cancer.
}}