{{Rsnum
|rsid=397507560
|Chromosome=9
|position=35074174
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CTGGATCCGT)
|geno3=(CTGGATCCGT;CTGGATCCGT)
|Gene=FANCG
|Gene_s=FANCG,VCP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=9
|CLNACC=RCV000007110.2
|CLNALLE=1
|CLNDBN=Fanconi anemia, complementation group G
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1401:CN069000:614082:84
|CLNHGVS=NC_000009.11:g.35074171_35074180delACGGATCCAG
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1401; 602956.0007
|Disease=Fanconi anemia
|FwdREF=TGGATCCGTC
|REF=GACGGATCCAG
|RSPOS=35074170
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397507560
|GENEINFO=VCP:7415; FANCG:2189
|GENE_ID=7415; 2189
|GENE_NAME=VCP; FANCG
}}