List of variants in gene BRSK2 reported as benign by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001256627.2(BRSK2):c.2188A>G (p.Thr730Ala)	rs4963048	0.68830
NM_001256627.2(BRSK2):c.-14C>T	rs112066837	0.52538
NM_001256627.2(BRSK2):c.1849+10C>T	rs67861777	0.21079
NM_001256627.2(BRSK2):c.564+13C>T	rs114665606	0.02477

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