ClinVar Miner

List of variants reported as pathogenic for chromosome 10 disorder by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_016628.5(WAC):c.1830_1833dup (p.Val612fs)
NM_016628.5(WAC):c.1864C>T (p.Arg622Ter)
NM_016628.5(WAC):c.284dup (p.Tyr95Ter)

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