{{Rsnum
|rsid=143149764
|Gene=B9D1
|Chromosome=17
|position=19347782
|Orientation=plus
|GMAF=0.0004591
|Gene_s=B9D1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=G
|CAF=0.9995; 0.0004591
|CHROM=17
|CLNACC=RCV000049798.1
|CLNALLE=1
|CLNDBN=not provided
|CLNHGVS=NC_000017.10:g.19251095A>G
|CLNSIG=4
|COMMON=0
|Disease=not provided
|FwdALT=G
|FwdREF=A
|GENEINFO=B9D1:27077
|GENE_ID=27077
|GENE_NAME=B9D1
|REF=A
|RSPOS=19251095
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000040016110100
|WGT=0
|dbSNPBuildID=134
|rsid=143149764
}}{{PMID Auto
|PMID=21493627
|Title=B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis.
|OA=1
}}