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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_024649.5(BBS1):c.1181G>A (p.Gly394Asp)	rs141528309	0.00096
NM_024649.5(BBS1):c.981C>T (p.Pro327=)	rs142243482	0.00011
NM_024649.5(BBS1):c.1634A>G (p.Asn545Ser)	rs148948642	0.00009
NM_024649.5(BBS1):c.858C>T (p.Ile286=)	rs746775716	0.00006
NM_024649.5(BBS1):c.840G>C (p.Lys280Asn)	rs780169168	0.00004
NM_024649.5(BBS1):c.1338C>T (p.Thr446=)	rs368302072	0.00003
NM_024649.5(BBS1):c.1371C>T (p.Tyr457=)	rs781014949	0.00003
NM_024649.5(BBS1):c.1626A>G (p.Pro542=)	rs780444865	0.00001
NM_024649.5(BBS1):c.1743C>T (p.His581=)	rs61890368	0.00001

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