Variants in gene NPC2 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006432.5(NPC2):c.212A>G (p.Lys71Arg)	rs142075589	0.00027
NM_006432.5(NPC2):c.450T>C (p.His150=)	rs374489111	0.00027
NM_006432.5(NPC2):c.292A>C (p.Asn98His)	rs142858704	0.00021
NM_006432.5(NPC2):c.270T>C (p.Pro90=)	rs758503440	0.00006
NM_006432.5(NPC2):c.264T>C (p.Pro88=)	rs1011669605	0.00003
NM_006432.5(NPC2):c.240C>T (p.Gly80=)	rs773836291	0.00001
NM_006432.5(NPC2):c.165C>T (p.Tyr55=)	rs2086712268
NM_006432.5(NPC2):c.414C>A (p.Leu138=)	rs1323196897

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