{{Rsnum
|rsid=1064074
|Gene=USH1C
|Chromosome=11
|position=17498195
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.4353
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=USH1C
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 39.7 | 36.5 | 23.8
| HCB | 11.1 | 28.9 | 60.0
| JPT | 2.3 | 52.3 | 45.5
| YRI | 17.7 | 53.2 | 29.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.1 | 28.9 | 60.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=1064074
|allele=G
|frequency=
|uid=1103649619897
|type=heterozygous_SNP
|hugo=USH1C
|ensembl gene=ENSG00000006611
|ensembl transcript=ENST00000318024
|sift=
|disease=Defects in USH1C are the cause of nonsyndromic recessive deafness (DFNB18) (MIM:602092).
}}

{{ClinVar
|rsid=1064074
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=17519742
|CHROM=11
|GMAF=0.4345
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x05016000000017051f100101
|GENEINFO=USH1C:10083
|GENE_NAME=USH1C
|GENE_ID=10083
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17519742C>G
|CLNORIGIN=1
|CLNSIG=2
|Tags=RV;PM;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.5647; 0.4353
|CLNACC=RCV000041279.1
|CLNDBN=AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|COMMON=1
|Disease=AllHighlyPenetrant
}}

{{GET Evidence
|gene=USH1C
|aa_change=Glu819Asp
|aa_change_short=E819D
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1064074
|overall_frequency_n=5557
|overall_frequency_d=10758
|overall_frequency=0.516546
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=59
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=3
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-2
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}