Variants in gene SMARCA4 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003072.5(SMARCA4):c.1351C>T (p.Arg451Cys)	rs2086534839
NM_003072.5(SMARCA4):c.2656A>G (p.Met886Val)	rs2146416371
NM_003072.5(SMARCA4):c.2704G>A (p.Val902Met)	rs1600278307
NM_003072.5(SMARCA4):c.2716C>T (p.Arg906Cys)	rs898406635
NM_003072.5(SMARCA4):c.2777A>G (p.Asn926Ser)	rs1555778797
NM_003072.5(SMARCA4):c.2896C>T (p.Arg966Trp)	rs1227826852
NM_003072.5(SMARCA4):c.3557C>T (p.Ala1186Val)	rs1600388982
NM_003072.5(SMARCA4):c.3608G>A (p.Arg1203His)	rs770680174
NM_003072.5(SMARCA4):c.3986G>A (p.Arg1329His)	rs1555785361

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