{{Rsnum
|rsid=10817610
|Gene=DFNB31
|Chromosome=9
|position=114426286
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.01423
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DFNB31
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 17.8 | 82.2
| ASW | 0.0 | 5.3 | 94.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 11.9 | 88.1
| MEX | 0.0 | 1.7 | 98.3
| MKK | 0.0 | 3.2 | 96.8
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=10817610
|allele=T
|frequency=1
|uid=1103652166774
|type=homozygous_SNP
|hugo=DFNB31
|ensembl gene=ENSG00000095397
|ensembl transcript=ENST00000362057
|sift=TOLERATED
|disease=Defects in WHRN are a cause of autosomal recessive deafness type 31 (DFNB31) (MIM:607084). This sensorineural hearing loss is bilateral and profound and manifests itself already in the prelingual period in early childhood.
}}

{{ClinVar
|rsid=10817610
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=117188566
|CHROM=9
|GMAF=0.0142
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x05016000000015051f100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.117188566C>T
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.01423; 0.9858
|COMMON=1
|GENEINFO=DFNB31:25861
|GENE_ID=25861
|GENE_NAME=DFNB31
|CLNACC=RCV000038858.1
|CLNDBN=AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|Disease=AllHighlyPenetrant
}}

{{GET Evidence
|gene=DFNB31
|aa_change=Arg364His
|aa_change_short=R364H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10817610
|overall_frequency_n=10550
|overall_frequency_d=10758
|overall_frequency=0.980666
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=107
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=1
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}