{{Rsnum
|rsid=76826147
|Gene=EPHB2
|Chromosome=1
|position=22913757
|Orientation=plus
|GMAF=0.0124
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=EPHB2
}}{{omim
|id=600997
|rsnum=76826147
|variant=0004
}}{{ClinVar
|rsid=76826147
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=22913757
|CHROM=1
|GMAF=0.0124
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160800005170516110100
|GENEINFO=EPHB2:2048
|GENE_NAME=EPHB2
|GENE_ID=2048
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.22913757A>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;SLO;U3;ASP;VLD;G5A;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9876; 0.0124
|CLNACC=RCV000009061.1
|CLNDBN=Prostate cancer, susceptibility to, in african americans
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_004442.6:c.*187A>T; 600997.0004
|COMMON=1
|Disease=Prostate cancer
}}