{{Rsnum
|rsid=104886003
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PIK3CA
|position=179218303
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PIK3CA
}}{{omim
|id=171834
|rsnum=104886003
|variant=0003
}}{{ClinVar
|rsid=104886003
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=178936091
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=3
|VP=0x050260000000000002110120
|GENEINFO=PIK3CA:5290
|GENE_NAME=PIK3CA
|GENE_ID=5290
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.178936091G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=2
|CLNSRCID=NBK153722; 171834.0003
|CLNSIG=255
|CLNCUI=C0677886
|CLNDBN=Breast adenocarcinoma; Ovarian epithelial cancer; Carcinoma of colon; Neoplasm of stomach; Keratosis, seborrheic, somatic; MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME, SOMATIC; Non-small cell lung cancer; Megalencephaly cutis marmorata telangiectatica congenita; Malignant melanoma
|Disease=Breast adenocarcinoma; Ovarian epithelial cancer; Carcinoma of colon; Neoplasm of stomach; Keratosis; MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; Non-small cell lung cancer; Megalencephaly cutis marmorata telangiectatica congenita; Malignant melanoma
|CLNACC=RCV000014631.1; RCV000014632.1; RCV000014633.1; RCV000014634.1; RCV000014636.1; RCV000032906.1; RCV000038671.3; RCV000055930.1; RCV000065935.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0858252; C0677886; C0699790:269533000; C0038356:613659:63443:126824007; C0007131:254637007; NBK153722:C1865285:602501:60040; C0025202:2092003
}}