Variants in gene MAN2B1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000528.4(MAN2B1):c.743C>T (p.Pro248Leu)	rs117843968	0.00237
NM_000528.4(MAN2B1):c.2865G>C (p.Thr955=)	rs148108322	0.00175
NM_000528.4(MAN2B1):c.1822G>A (p.Glu608Lys)	rs145062583	0.00139
NM_000528.4(MAN2B1):c.2260G>A (p.Glu754Lys)	rs141212446	0.00132
NM_000528.4(MAN2B1):c.1230+9G>C	rs367590716	0.00078
NM_000528.4(MAN2B1):c.1521G>T (p.Ala507=)	rs143318498	0.00077
NM_000528.4(MAN2B1):c.1158G>A (p.Gln386=)	rs112829030	0.00025
NM_000528.4(MAN2B1):c.2670A>G (p.Ser890=)	rs199606152	0.00010
NM_000528.4(MAN2B1):c.2782G>C (p.Gly928Arg)	rs754733253	0.00006
NM_000528.4(MAN2B1):c.1231-13C>T	rs372848519
NM_000528.4(MAN2B1):c.2267+8dup	rs572289342

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