{{Rsnum
|rsid=397515481
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR1
|position=38428048
|Gene_s=FGFR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=8
|CLNACC=RCV000056314.26
|CLNALLE=1
|CLNDBN=Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1530:C1845146:300571
|CLNHGVS=NC_000008.10:g.38285566A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=136350.0031
|Disease=Holoprosencephaly
|FwdALT=C
|FwdREF=T
|GENEINFO=FGFR1:2260
|GENE_ID=2260
|GENE_NAME=FGFR1
|REF=A
|RSPOS=38285566
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515481
}}