{{Rsnum
|rsid=137853247
|Gene=HNF1A
|Chromosome=12
|position=120978860
|Orientation=plus
|GMAF=0.0004591
|Gene_s=HNF1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=142410
|variant=0022
|rsnum=137853247
}}{{ClinVar
|rsid=137853247
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=121416663
|CHROM=12
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=HNF1A:6927
|GENE_NAME=HNF1A
|GENE_ID=6927
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.121416663G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142410.0022
|CLNSIG=5
|CLNCUI=C1838100
|CLNDBN=Maturity-onset diabetes of the young, type 3; Clear cell carcinoma of kidney; Chromophobe renal cell carcinoma
|Disease=Maturity-onset diabetes of the young; Clear cell carcinoma of kidney; Chromophobe renal cell carcinoma
|CLNACC=RCV000016086.20; RCV000016087.20; RCV000016088.20
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:SNOMED_CT:SNOMED_CT; MedGen
|CLNDSDBID=C1838100:600496:552; C0279702:188251003:254915003; C1266042
|COMMON=0
}}