Variants with conflicting interpretations "likely pathogenic" from National Institute of Mental Health and Neurosciences and "pathogenic" from any submitter

Minimum review status of the submission from National Institute of Mental Health and Neurosciences:		Collection method of the submission from National Institute of Mental Health and Neurosciences:
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_000159.4(GCDH):c.1031C>T (p.Thr344Ile)	rs869025299
NM_000159.4(GCDH):c.1173del (p.Asn392fs)	rs754002357

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