{{Rsnum
|rsid=151344539
|Chromosome=12
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=HNF1A
|position=120999086
|Gene_s=HNF1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=151344539
|Reversed=0
|FwdALT=G
|REF=T
|ALT=TG
|RSPOS=121436889
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050068080001000002110200
|GENEINFO=HNF1A:6927
|GENE_NAME=HNF1A
|GENE_ID=6927
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.121436889_121436890insG
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611101.0001; 611101.0001; 611101.0001; 611101.0001
|CLNSIG=1
|CLNCUI=C1970211; C1970211; C1970211; C1970211
|CLNDBN=Distal spinal muscular atrophy, autosomal recessive 4
|Disease=Distal spinal muscular atrophy
|CLNACC=SCV000021224.1; SCV000021224.1; SCV000021224.1; SCV000021224.1
|Tags=PM;PMC;INT;OTHERKG;LSD;OM
}}{{PMID|19794065|OA=1
}} Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes.