ClinVar Miner

List of variants reported as pathogenic for chromosome 18p deletion syndrome by Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 18p11.32-11.22(chr18:136226-10172941)
GRCh37/hg19 18p11.32-11.23(chr18:136226-7131132)

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