ClinVar Miner

List of variants reported as likely pathogenic for Thyroid hemiagenesis

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Total variants: 9
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HGVS dbSNP
GRCh37/hg19 11p15.2(chr11:14504463-14909461)x1
GRCh37/hg19 11p15.2(chr11:14657389-14918308)x1
GRCh37/hg19 14q23.1(chr14:58737402-58884615)x1
GRCh37/hg19 14q23.1(chr14:58737402-58891576)x1
GRCh37/hg19 15q22.2(chr15:62128861-62340126)x1
GRCh37/hg19 15q22.2(chr15:62155282-62332980)x1
GRCh37/hg19 17q21.1(chr17:38146929-38153473)x1
GRCh37/hg19 2p21(chr2:45453858-45455897)x3
GRCh37/hg19 2p21(chr2:45454554-45457111)x3

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