{{Rsnum
|rsid=180177085
|Chromosome=16
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=PALB2
|position=23636151
|Gene_s=PALB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNALLE=1
|CLNDBN=Fanconi anemia, complementation group N
|CLNDSDB=OMIM
|CLNDSDBID=610832
|CLNHGVS=NC_000016.9:g.23647472delA
|CLNORIGIN=1
|CLNSIG=5
|Disease=Fanconi anemia
|FwdREF=T
|GENEINFO=PALB2:79728
|GENE_ID=79728
|GENE_NAME=PALB2
|REF=GA
|RSPOS=23647471
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068001201000002110200
|WGT=1
|dbSNPBuildID=135
|rsid=180177085
}}{{PMID Auto
|PMID=17200671
|Title=Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
}}