Variants with conflicting interpretations "pathogenic" from Human Genome Lab, NIMHANS, National Institute of Mental Health and Neuro Sciences and "likely pathogenic" from any submitter

Minimum review status of the submission from Human Genome Lab, NIMHANS, National Institute of Mental Health and Neuro Sciences:		Collection method of the submission from Human Genome Lab, NIMHANS, National Institute of Mental Health and Neuro Sciences:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000454.5(SOD1):c.262G>A (p.Val88Met)	rs1568810641
NM_000454.5(SOD1):c.43G>A (p.Val15Met)	rs1568807400
NM_000454.5(SOD1):c.43G>C (p.Val15Leu)	rs1568807400
NM_001377265.1(MAPT):c.2179G>A (p.Gly727Ser)	rs63750095

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