Related gene-specific medical variations for Gene (Select 9577) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2650777	NM_199191.3(BABAM2):c.1088+11589A>C	BABAM2, LOC100505716 +1 more	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 979975	GRCh37/hg19 2p23.2(chr2:28180918-28304630)x1	BABAM2	Copy number loss	not provided	GUncertain significance
Select item 161855	NM_199191.3(BABAM2):c.626A>G (p.Asp209Gly)	BABAM2 (D209G)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance

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