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#fileformat=VCFv4.1 | |
#fileDate=2019-03-01 | |
#source=ClinVar | |
#reference=GRCh38 | |
#ID=<Description="ClinVar Variation ID"> | |
#INFO=<ID=AF_ESP,Number=1,Type=Float,Description="allele frequencies from GO-ESP"> | |
#INFO=<ID=AF_EXAC,Number=1,Type=Float,Description="allele frequencies from ExAC"> | |
#INFO=<ID=AF_TGP,Number=1,Type=Float,Description="allele frequencies from TGP"> | |
#INFO=<ID=ALLELEID,Number=1,Type=Integer,Description="the ClinVar Allele ID"> | |
#INFO=<ID=CLNDN,Number=.,Type=String,Description="ClinVar's preferred disease name for the concept specified by disease identifiers in CLNDISDB"> |
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