Variants in gene combination BBS1, ZDHHC24 with conflicting interpretations reported as "uncertain significance and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_024649.5(BBS1):c.1110+329C>T	rs571170303	0.00002
NM_024649.5(BBS1):c.1110G>A (p.Pro370=)	rs183771956	0.00002
NM_024649.5(BBS1):c.1553T>C (p.Leu518Pro)	rs121917778	0.00001
NM_024649.5(BBS1):c.1205T>C (p.Leu402Pro)	rs767150997
NM_024649.5(BBS1):c.1570_1572del (p.Asn524del)	rs863224782
NM_024649.5(BBS1):c.1717C>T (p.Gln573Ter)	rs1450045618

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