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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 16

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HGVS	dbSNP	gnomAD frequency
NM_024649.5(BBS1):c.1169T>G (p.Met390Arg)	rs113624356	0.00212
NM_024649.5(BBS1):c.1645G>T (p.Glu549Ter)	rs121917777	0.00012
NM_024649.5(BBS1):c.1339G>A (p.Ala447Thr)	rs200116631	0.00003
NM_024649.5(BBS1):c.724-1G>C	rs748523268	0.00003
NM_024649.5(BBS1):c.1318C>T (p.Arg440Ter)	rs1014835928	0.00001
NM_024649.5(BBS1):c.1553T>C (p.Leu518Pro)	rs121917778	0.00001
NM_024649.5(BBS1):c.1097T>A (p.Val366Asp)
NM_024649.5(BBS1):c.1110+3G>C	rs762276925
NM_024649.5(BBS1):c.1131_1135del (p.Cys377fs)	rs786204701
NM_024649.5(BBS1):c.1285C>T (p.Arg429Ter)	rs768443448
NM_024649.5(BBS1):c.1340-1G>T	rs1555049893
NM_024649.5(BBS1):c.1340-2A>G	rs113994180
NM_024649.5(BBS1):c.1570_1572del (p.Asn524del)	rs863224782
NM_024649.5(BBS1):c.1643dup (p.Glu549fs)	rs773632109
NM_024649.5(BBS1):c.1708C>T (p.Arg570Ter)	rs1434577015
NM_024649.5(BBS1):c.951+1G>A	rs746875134

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