{{Rsnum
|rsid=121434567
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EGF
|position=110004540
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EGF
}}{{omim
|id=131530
|rsnum=121434567
|variant=0001
}}{{ClinVar
|rsid=121434567
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=110925696
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=EGF:1950
|GENE_NAME=EGF
|GENE_ID=1950
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.110925696C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=131530.0001
|CLNSIG=5
|CLNCUI=C2673648
|CLNDBN=Hypomagnesemia 4, renal
|Disease=Hypomagnesemia 4
|CLNACC=RCV000018089.26
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2673648:611718:34527
}}