{{Rsnum
|rsid=398123006
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GRHL2
|position=101631636
|Gene_s=GRHL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000077792.1
|CLNALLE=1
|CLNDBN=Deafness, autosomal dominant 28
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1837640:608641:90635
|CLNHGVS=NC_000008.10:g.102643864G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608576.0002
|Disease=Deafness
|FwdALT=A
|FwdREF=G
|GENEINFO=GRHL2:79977
|GENE_ID=79977
|GENE_NAME=GRHL2
|REF=G
|RSPOS=102643864
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398123006
}}