{{Rsnum
|rsid=121434425
|Chromosome=9
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FANCG
|position=35078338
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FANCG
}}{{omim
|id=602956
|rsnum=121434425
|variant=0001
}}{{ClinVar
|rsid=121434425
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=35078335
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FANCG:2189
|GENE_NAME=FANCG
|GENE_ID=2189
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.35078335C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602956.0001
|CLNSIG=5
|CLNCUI=CN069000
|CLNDBN=Fanconi anemia, complementation group G
|Disease=Fanconi anemia
|CLNACC=RCV000007104.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1401:CN069000:614082:84
}}