{{Rsnum
|rsid=119462978
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KIRREL3
|position=126562850
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KIRREL3
}}{{omim
|id=607761
|rsnum=119462978
|variant=0001
}}{{ClinVar
|rsid=119462978
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=126432745
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=KIRREL3:84623
|GENE_NAME=KIRREL3
|GENE_ID=84623
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.126432745G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607761.0001
|CLNSIG=5
|CLNCUI=C2675487
|CLNDBN=Mental retardation, autosomal dominant 4
|Disease=Mental retardation
|CLNACC=RCV000003020.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2675487:612581
}}