List of variants in gene SMARCA4 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_003072.5(SMARCA4):c.4635+12G>A	rs34930626	0.01001
NM_003072.5(SMARCA4):c.2002-19T>C	rs111899994	0.00578
NM_003072.5(SMARCA4):c.222+14T>C	rs112825147	0.00548
NM_003072.5(SMARCA4):c.222+18C>T	rs180832203	0.00381
NM_003072.5(SMARCA4):c.2275-3C>A	rs117611401	0.00243
NM_003072.5(SMARCA4):c.4170+17C>T	rs145829956

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