Variants in gene BBS2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 4

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HGVS	dbSNP	gnomAD frequency
NM_031885.5(BBS2):c.805-20A>G	rs41280892	0.00423
NM_031885.5(BBS2):c.1422G>A (p.Ser474=)	rs117033008	0.00250
NM_031885.5(BBS2):c.126T>G (p.Ile42Met)	rs139945733	0.00061
NM_031885.5(BBS2):c.266A>G (p.Tyr89Cys)	rs560910758

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