{{Rsnum
|rsid=1800111
|Gene=CFTR
|Chromosome=7
|position=117610521
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=1800111
|variant=0124
}}{{ClinVar
|rsid=1800111
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=117250575
|CHROM=7
|GMAF=0.0018
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050168000000040116110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117250575G>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNACC=RCV000007650.1; RCV000007651.1; RCV000046745.2; RCV000078991.1
|CLNDBN=Pancreatitis, idiopathic, susceptibility to; Hypertrypsinemia, neonatal, susceptibility to; Cystic fibrosis; not provided
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNSRCID=259; 602421.0124
|COMMON=1
|Disease=Pancreatitis; Hypertrypsinemia; Cystic fibrosis; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}{{PMID Auto
|PMID=18716917
|Title=A novel computational and structural analysis of nsSNPs in CFTR gene.
|OA=1
}}