Related gene-specific medical variations for Gene (Select 9529) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3132824	NM_001015048.3(BAG5):c.-29+694C>G	BAG5, LOC130056586	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2291157	NM_001015048.3(BAG5):c.-29+693C>T	BAG5, LOC130056586	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance