Variants with conflicting interpretations "likely pathogenic" from Clinical Genetics and Genomics, Karolinska University Hospital and "likely benign" from any submitter

Minimum review status of the submission from Clinical Genetics and Genomics, Karolinska University Hospital:		Collection method of the submission from Clinical Genetics and Genomics, Karolinska University Hospital:
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_000451.4(SHOX):c.-55C>T	rs772910213	0.00401
NM_001349253.2(SCN11A):c.3473T>C (p.Leu1158Pro)	rs141686175	0.00047
NM_014804.3(KIAA0753):c.810C>T (p.Tyr270=)	rs752659088	0.00006

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