{{Rsnum
|rsid=121913322
|Gene=STK11
|Chromosome=19
|position=1221320
|Orientation=plus
|GMAF=0.001837
|Gene_s=STK11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}Simple Nucleotide Polymorphisms (dbSNP 135) Flagged by dbSNP as Clinically Associatied SNP

From UCSC hg19 Position: chr19:1221319-1221319
http://main.genome-browser.bx.psu.edu/cgi-bin/hgc?hgsid=147742&c=chr19&o=1221318&t=1221319&g=snp135Flagged&i=rs121913322

Summary: C>C/T;
chimp allele displayed first, then '>', then human alleles;

Strand: +; Observed: C/T;
UCSC Reference allele: 	C
				
Chimp allele: 	C	   Chimp strand: 	+	   Chimp position: 	chr19:1171245-1171245;

Orangutan allele: 	C	   Orangutan strand: 	+	   Orangutan position: 	chr19:1137481-1137481;

Macaque allele: 	C	   Macaque strand: 	+	   Macaque position: 	chr19:975254-975254;

Class	single

Validation	by-cluster,by-1000genomes; 
Function	missense_variant; 
Molecule Type  	genomic; 
Weight	1;

Submitter Handles:  	1000GENOMES, DF-BWCC;

1000 genome Allele Frequencies:  	C: 99.817% (2184 / 2188); T: 0.183% (4 / 2188);
MAF/MinorAlleleCount:	T=0.002/4;
MAF Source:	1000 Genomes;

Miscellaneous properties annotated by dbSNP: 

SNP is in OMIM/OMIA and/or at least one submitter is a Locus-Specific Database ("clinically associated") ;
SNP was submitted by Locus-Specific Database; 

Coding annotations by dbSNP:
STK11 (NM_000455): missense_variant P (CCG) --> L (CTG);

dbSNP: rs121913322

http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=121913322

ss275515168	DF-BWCC|Cosmic:21355
ss491143638	1000GENOMES|20110521_exome_651436_chr19_1221319
ss491143638	1000GENOMES|20110521_exome_651436_chr19_1221319
ss491535737	EXOME_CHIP|nonsyn_251963_chr_19_1221319{{ClinVar
|ALT=T
|CAF=0.9982; 0.001837
|CHROM=19
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.1221319C>T
|CLNORIGIN=2
|CLNSIG=1
|COMMON=1
|FwdALT=T
|FwdREF=C
|GENEINFO=STK11:6794
|GENE_ID=6794
|GENE_NAME=STK11
|REF=C
|RSPOS=1221319
|Reversed=0
|SAO=3
|SSR=0
|Tags=PM;S3D;NSM;REF;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050260000a01000016100120
|WGT=1
|dbSNPBuildID=133
|rsid=121913322
}}