Variants in gene CENPJ with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_018451.5(CENPJ):c.163C>G (p.Pro55Ala)	rs17081389	0.02639
NM_018451.5(CENPJ):c.187G>C (p.Asp63His)	rs7336216	0.02151
NM_018451.5(CENPJ):c.287A>G (p.His96Arg)	rs61739263	0.01206
NM_018451.5(CENPJ):c.1233G>A (p.Pro411=)	rs112133852	0.00368
NM_018451.5(CENPJ):c.175A>G (p.Thr59Ala)	rs138732534	0.00157
NM_018451.5(CENPJ):c.2806A>G (p.Ser936Gly)	rs75008861	0.00070
NM_018451.5(CENPJ):c.2462C>T (p.Thr821Met)	rs144938364	0.00056
NM_018451.5(CENPJ):c.763A>G (p.Thr255Ala)	rs150932292	0.00053
NM_018451.5(CENPJ):c.1430C>T (p.Thr477Met)	rs193181742	0.00014
NM_018451.5(CENPJ):c.810A>G (p.Gln270=)	rs572213217	0.00001
NM_018451.5(CENPJ):c.1908C>G (p.Arg636=)	rs61743613
NM_018451.5(CENPJ):c.2992-17dup	rs35599563
NM_018451.5(CENPJ):c.2992-18_2992-17del	rs151246139
NM_018451.5(CENPJ):c.2992-6del	rs35599563

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