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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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.1408C>T (p.Gln470Ter)	rs1555757738
NM_003072.5(SMARCA4):c.1757_1760del (p.Lys586fs)	rs1342399494
NM_003072.5(SMARCA4):c.229G>T (p.Glu77Ter)	rs1568419675
NM_003072.5(SMARCA4):c.2653C>T (p.Arg885Cys)	rs281875227
NM_003072.5(SMARCA4):c.2851G>A (p.Gly951Arg)	rs1060499936
NM_003072.5(SMARCA4):c.2933G>A (p.Arg978Gln)	rs1180804356
NM_003072.5(SMARCA4):c.2936G>A (p.Arg979Gln)
NM_003072.5(SMARCA4):c.3127C>T (p.Arg1043Trp)	rs770014321
NM_003072.5(SMARCA4):c.3229C>T (p.Arg1077Ter)	rs2146541571

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