{{Rsnum
|rsid=121434382
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HMCN1
|position=186178506
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HMCN1
}}{{omim
|id=608548
|rsnum=121434382
|variant=0001
}}{{ClinVar
|rsid=121434382
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=186178506
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05040002110100
|GENEINFO=HMCN1:83872
|GENE_NAME=HMCN1
|GENE_ID=83872
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.186178506A>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|CLNACC=RCV000002289.1
|CLNDBN=MACULAR DEGENERATION, AGE-RELATED, 1, SUSCEPTIBILITY TO
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_031935.2:c.16034A>G; 608548.0001
|Disease=MACULAR DEGENERATION
}}