List of variants in gene BRAT1 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_152743.4(BRAT1):c.128-10A>G	rs2164688	0.46043
NM_152743.4(BRAT1):c.2388A>G (p.Glu796=)	rs1043291	0.45840
NM_152743.4(BRAT1):c.1932A>G (p.Arg644=)	rs4719552	0.45541
NM_152743.4(BRAT1):c.2209C>T (p.Arg737Trp)	rs60152725	0.02491
NM_152743.4(BRAT1):c.1206C>T (p.Asp402=)	rs7807895	0.01413
NM_152743.4(BRAT1):c.993G>A (p.Thr331=)	rs76646873	0.00653
NM_152743.4(BRAT1):c.1884C>T (p.Ala628=)	rs142346283	0.00625
NM_152743.4(BRAT1):c.675C>T (p.Phe225=)	rs139443843	0.00438
NM_152743.4(BRAT1):c.1579C>T (p.Leu527=)	rs151161353	0.00126
NM_152743.4(BRAT1):c.1931_1932delinsAG (p.Arg644Gln)	rs71531463

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