{{Rsnum
|rsid=137853139
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KRIT1
|position=92236488
|Gene_s=KRIT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=604214
|variant=0008
|rsnum=137853139
}}{{ClinVar
|rsid=137853139
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=91865802
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=KRIT1:889
|GENE_NAME=KRIT1
|GENE_ID=889
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.91865802T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604214.0008
|CLNSIG=5
|CLNCUI=CN042719
|CLNDBN=Cerebral cavernous malformations 1
|Disease=Cerebral cavernous malformations 1
|CLNACC=RCV000006079.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1293:CN042719
}}