{{Rsnum
|rsid=111033592
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WNK1
|position=868046
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNK1
}}{{omim
|id=605232
|rsnum=111033592
|variant=0007
}}
{{omim
|id=605232
|rsnum=111033592
|variant=0009
}}{{ClinVar
|rsid=111033592
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=977212
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=WNK1:65125
|GENE_NAME=WNK1
|GENE_ID=65125
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.977212C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000005471.1
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY, TYPE II
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605232.0009
|Disease=NEUROPATHY
}}