{{Rsnum
|rsid=1135101
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226788
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=1135101
|variant=0516
}}{{ClinVar
|rsid=1135101
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=5248018
|CHROM=11
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5248018A>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016872.1
|CLNDBN=HEMOGLOBIN SANTANDER
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=1160; 141900.0516
|Disease=HEMOGLOBIN SANTANDER
}}{{PMID Auto
|PMID=12603091
|Title=Hb Santander [beta34(B16)Val --> Asp (GTC --> GAC)]: a new unstable variant found as a de novo mutation in a Spanish patient.
}}