{{Rsnum
|rsid=59912467
|Gene=STK11
|Chromosome=19
|position=1223126
|Orientation=plus
|GMAF=0.01286
|Gene_s=STK11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=59912467
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=1223125
|CHROM=19
|GMAF=0.0128
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000170416110100
|GENEINFO=STK11:6794
|GENE_NAME=STK11
|GENE_ID=6794
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.1223125C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602216.0024
|CLNSIG=5
|CLNCUI=C0031269
|CLNDBN=Peutz-Jeghers syndrome
|Disease=Peutz-Jeghers syndrome
|CLNACC=RCV000007887.2
|Tags=PM;VLD;G5A;G5;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9871; 0.01286
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1266:C0031269:175200:2869:54411001
|COMMON=1
}}

{{GET Evidence
|gene=STK11
|aa_change=Phe354Leu
|aa_change_short=F354L
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs59912467
|overall_frequency_n=42
|overall_frequency_d=10566
|overall_frequency=0.00397501
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|pph2_score=0.021
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=4
|webscore=N
|n_web_uneval=10
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}