{{Rsnum
|rsid=111033590
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WNK1
|position=868772
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNK1
}}{{omim
|id=605232
|rsnum=111033590
|variant=0005
}}
{{omim
|id=201300
|rsnum=111033590
}}
{{omim
|id=605232
|rsnum=111033590
|variant=0003
}}{{ClinVar
|rsid=111033590
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=977938
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=WNK1:65125
|GENE_NAME=WNK1
|GENE_ID=65125
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.977938C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000005473.1; RCV000020433.1
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY, TYPE II; Hereditary sensory and autonomic neuropathy type IIA
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK49247:C2752089:201300:970
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK49247; 605232.0005
|Disease=NEUROPATHY; Hereditary sensory and autonomic neuropathy type IIA
}}