{{Rsnum
|rsid=113993958
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=7
|Orientation=plus
|Gene=CFTR
|position=117530953
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}[[rs113993958]] in the [[CFTR]] gene potentially leading to a mild form of [[cystic fibrosis]] known as D110H ([http://www.ncbi.nlm.nih.gov/omim/602421#602421Variants0004 OMIM 602041.0004]). The common form is [[rs113993958]](G), whereas the form leading (when present in two copies) to cystic fibrosis is [[rs113993958]](C).
{{omim
|id=602421
|rsnum=113993958
|variant=0004
}}{{ClinVar
|rsid=113993958
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=117171007
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.117171007G>C; NC_000007.13:g.117171007G>T
|CLNSRC=CFTR2; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=D110H; 602421.0004
|CLNSIG=5
|CLNCUI=C0010674
|CLNDBN=Cystic fibrosis; not provided
|Disease=Cystic fibrosis; not provided
|CLNACC=RCV000007527.3; RCV000058930.1; RCV000046852.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}