{{Rsnum
|rsid=61736451
|Gene=ATP2B2
|Chromosome=3
|position=10359892
|Orientation=plus
|GMAF=0.006428
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATP2B2
}}{{omim
|id=108733
|rsnum=61736451
|variant=0001
}}{{ClinVar
|rsid=61736451
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=10401576
|CHROM=3
|GMAF=0.0064
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000040116110100
|GENEINFO=ATP2B2:491
|GENE_NAME=ATP2B2
|GENE_ID=491
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.10401576C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9936; 0.006428
|CLNACC=RCV000019379.22
|CLNDBN=Deafness, autosomal recessive 12, modifier of
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=108733.0001
|COMMON=1
|Disease=Deafness
}}{{GET Evidence
|gene=ATP2B2
|aa_change=Val631Met
|aa_change_short=V631M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs61736451
|overall_frequency_n=59
|overall_frequency_d=10758
|overall_frequency=0.00548429
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=1
|webscore=N
}}