List of variants in gene SMARCA4 reported as benign by Genetic Services Laboratory, University of Chicago

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_003072.5(SMARCA4):c.1524T>C (p.His508=)	rs7935	0.32239
NM_003072.5(SMARCA4):c.4887T>C (p.Asp1629=)	rs7275	0.28266
NM_003072.5(SMARCA4):c.4053C>T (p.Asp1351=)	rs28997582	0.04598
NM_003072.5(SMARCA4):c.1419+7T>C	rs112977340	0.00546
NM_003072.5(SMARCA4):c.2001+8T>G	rs112549813	0.00384
NM_003072.5(SMARCA4):c.1140C>T (p.His380=)	rs114594206	0.00372
NM_003072.5(SMARCA4):c.589C>T (p.Pro197Ser)	rs200664441	0.00291
NM_003072.5(SMARCA4):c.2275-3C>A	rs117611401	0.00243
NM_003072.5(SMARCA4):c.2757C>T (p.Pro919=)	rs113955216	0.00241
NM_003072.5(SMARCA4):c.981A>C (p.Pro327=)	rs547268941	0.00233
NM_003072.5(SMARCA4):c.*1G>T	rs76118382	0.00205
NM_003072.5(SMARCA4):c.4768+10G>A	rs201665695	0.00200
NM_003072.5(SMARCA4):c.3045C>T (p.Gly1015=)	rs56101423	0.00163
NM_003072.5(SMARCA4):c.3738C>T (p.Phe1246=)	rs139943231	0.00039
NM_003072.5(SMARCA4):c.441C>T (p.Ser147=)	rs201372858	0.00016
NM_003072.5(SMARCA4):c.3066C>T (p.Ser1022=)	rs149111403	0.00003
NM_003072.5(SMARCA4):c.120C>T (p.His40=)	rs375884151

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