C1865270[trait identifier] AND "Baylor-Hopkins Center for Mendelian Ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4388	NM_057176.3(BSND):c.35T>C (p.Ile12Thr)	BSND (I12T)	Single nucleotide variant (missense variant)	Bartter syndrome +2 more	GConflicting classifications of pathogenicity
Select item 634810	NM_057176.3(BSND):c.52C>G (p.Leu18Val)	BSND (L18V)	Single nucleotide variant (missense variant)	Bartter disease type 4A	GUncertain significance