List of variants in gene BSND reported as benign for Bartter syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_057176.3(BSND):c.*175C>G	rs4339899	0.46025
NM_057176.3(BSND):c.924G>A (p.Pro308=)	rs33938617	0.18512
NM_057176.3(BSND):c.127G>A (p.Val43Ile)	rs34561376	0.04587

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