{{Rsnum
|rsid=1136743
|Gene=SAA1
|Chromosome=11
|position=18269312
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.4761
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SAA1
}}{{Venter SNP
|rsid=1136743
|allele=T
|frequency=
|uid=1103649621118
|type=homozygous_SNP
|hugo=SAA1
|ensembl gene=ENSG00000173432
|ensembl transcript=ENST00000356524
|sift=TOLERATED
|disease=TH is from a patient with juvenile rheumatoid arthritis.
}}
{{ neighbor
| rsid = 1136747
| distance = 15
}}
{{ neighbor
| rsid = 17856195
| distance = 1
}}
{{omim
|id=104750
|rsnum=1136743
|variant=0002
}}{{ClinVar
|rsid=1136743
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=18290859
|CHROM=11
|GMAF=0.4757
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x050168000000150116110100
|GENEINFO=SAA1:6288
|GENE_NAME=SAA1
|GENE_ID=6288
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.18290859C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;SLO;VLD;G5;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.5239; 0.4761
|CLNACC=RCV000019736.26
|CLNDBN=Serum amyloid a variant
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=104750.0002
|COMMON=1
|Disease=Serum amyloid a variant
}}{{PMID Auto
|PMID=18389087
|Title=Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing.
|OA=1
}}