Variants in gene BBS10 with conflicting interpretations "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: 14

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HGVS	dbSNP	gnomAD frequency
NM_024685.4(BBS10):c.1736A>G (p.Lys579Arg)	rs141521925	0.00159
NM_024685.4(BBS10):c.765G>A (p.Met255Ile)	rs139658279	0.00072
NM_024685.4(BBS10):c.1436C>A (p.Ala479Glu)	rs138434761	0.00058
NM_024685.4(BBS10):c.886G>A (p.Ala296Thr)	rs150587582	0.00041
NM_024685.4(BBS10):c.372T>A (p.Ser124=)	rs143366878	0.00014
NM_024685.4(BBS10):c.1590A>C (p.Arg530Ser)	rs146812823	0.00010
NM_024685.4(BBS10):c.1333C>A (p.Leu445Ile)	rs199878555	0.00009
NM_024685.4(BBS10):c.440A>G (p.Gln147Arg)	rs140585012	0.00006
NM_024685.4(BBS10):c.42G>A (p.Ala14=)	rs373458861	0.00005
NM_024685.4(BBS10):c.462G>A (p.Leu154=)	rs764687344	0.00003
NM_024685.4(BBS10):c.483A>G (p.Lys161=)	rs748732850	0.00001
NM_024685.4(BBS10):c.1158G>A (p.Leu386=)	rs138702315
NM_024685.4(BBS10):c.147G>A (p.Arg49=)	rs1592493118
NM_024685.4(BBS10):c.1684T>C (p.Leu562=)	rs111773727

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