ClinVar Miner

List of variants reported as likely pathogenic by Reutter Lab, Institute of Human Genetics,University Hospital Bonn

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Total variants: 5
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HGVS dbSNP
GRCh37/hg19 10q11.21(chr10:43796180-44037408)x3
GRCh37/hg19 16q23.3(chr16:83414018-83518410)x1
GRCh37/hg19 22q11.21(chr22:18915347-21463730)x1
GRCh37/hg19 5q23.1(chr5:118890915-119082631)x1
NM_001451.3(FOXF1):c.658G>T (p.Gly220Cys) rs752504125

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