ClinVar Miner

List of variants studied for primary hypertrophic osteoarthropathy by Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg

Included ClinVar conditions (6):

Cranioosteoarthropathy
Hypertrophic osteoarthropathy, primary, autosomal dominant
Hypertrophic osteoarthropathy, primary, autosomal recessive, 1
Hypertrophic osteoarthropathy, primary, autosomal recessive, 2
Isolated congenital digital clubbing; Hypertrophic osteoarthropathy, primary, autosomal recessive, 1
Pachydermoperiostosis syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_000860.6(HPGD):c.662+2T>A

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