Variants with conflicting interpretations "likely pathogenic" from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University and "pathogenic" from any submitter

Minimum review status of the submission from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University:		Collection method of the submission from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.838G>T (p.Asp280Tyr)	rs119103226	0.00001
NM_001165963.4(SCN1A):c.4601T>A (p.Val1534Asp)	rs2105449751
NM_015506.3(MMACHC):c.89G>A (p.Trp30Ter)	rs1570829502
Single allele

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