Variants with conflicting interpretations "likely pathogenic" from HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP) and "uncertain significance" from any submitter

Minimum review status of the submission from HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP):		Collection method of the submission from HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP):
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6899G>C (p.Trp2300Ser)	rs1555119899
NM_000540.3(RYR1):c.14809A>G (p.Ile4937Val)	rs2145917369

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