ClinVar Miner

List of variants reported as benign for hematologic disorder by The Clinical Immunogenomics Research Consortium Australasia, Garvan Institute of Medical Research

Included ClinVar conditions (812):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.3234+2T>C rs756871628 0.00010

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