{{Rsnum
|rsid=121913662
|Chromosome=2
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NEB
|position=151490495
|Gene_s=NEB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=161650
|rsnum=121913662
|variant=0005
}}{{ClinVar
|rsid=121913662
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=152347009
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NEB:4703
|GENE_NAME=NEB
|GENE_ID=4703
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.152347009C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=161650.0005
|CLNSIG=5
|CLNCUI=C1850569
|CLNDBN=Nemaline myopathy 2
|Disease=Nemaline myopathy 2
|CLNACC=RCV000015094.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1288:C1850569:256030:607
}}