{{Rsnum
|rsid=398122997
|Chromosome=8
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=GRHL2
|position=101644222
|Gene_s=GRHL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GC
|CHROM=8
|CLNACC=RCV000002279.2
|CLNALLE=1
|CLNDBN=Deafness, autosomal dominant 28
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1837640:608641:90635
|CLNHGVS=NC_000008.10:g.102656450dupC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608576.0001
|Disease=Deafness
|FwdALT=C
|GENEINFO=GRHL2:79977
|GENE_ID=79977
|GENE_NAME=GRHL2
|REF=G
|RSPOS=102656449
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398122997
}}