{{Rsnum
|rsid=121918202
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RPGRIP1L
|position=53671580
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RPGRIP1L
}}{{omim
|id=610937
|rsnum=121918202
|variant=0006
}}{{ClinVar
|rsid=121918202
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=53705492
|CHROM=16
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RPGRIP1L:23322
|GENE_NAME=RPGRIP1L
|GENE_ID=23322
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.53705492G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610937.0006
|CLNSIG=5
|CLNCUI=C1969052
|CLNDBN=Meckel syndrome type 5
|Disease=Meckel syndrome type 5
|CLNACC=RCV000001128.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1969052:611561:564
}}