{{Rsnum
|rsid=28941780
|Gene=CRELD1
|Chromosome=3
|position=9937624
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CRELD1
}}{{omim
|desc=ATRIOVENTRICULAR SEPTAL DEFECT, PARTIAL, WITH HETEROTAXY SYNDROME
|id=607170
|rsnum=28941780
|variant=0003
}}{{ClinVar
|rsid=28941780
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=9979308
|CHROM=3
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=CRELD1:78987
|GENE_NAME=CRELD1
|GENE_ID=78987
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.9979308G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000003598.1
|CLNDBN=Atrioventricular septal defect, partial, with heterotaxy syndrome
|CLNDSDB=MedGen
|CLNDSDBID=C1853509
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607170.0003
|COMMON=0
|Disease=Atrioventricular septal defect
}}