Variants with conflicting interpretations "likely pathogenic" from CeGaT Center for Human Genetics Tuebingen and "drug response" from any submitter

Minimum review status of the submission from CeGaT Center for Human Genetics Tuebingen:		Collection method of the submission from CeGaT Center for Human Genetics Tuebingen:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001025195.2(CES1):c.431G>A (p.Gly144Glu)	rs71647871	0.00998
NM_000540.3(RYR1):c.7007G>A (p.Arg2336His)	rs112563513	0.00001
NM_000540.3(RYR1):c.7282G>A (p.Ala2428Thr)	rs193922809	0.00001

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