Related gene-specific medical variations for Gene (Select 414061) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2250866	NM_001072.4(UGT1A6):c.862-23503A>T	DNAJB3, UGT1A +8 more	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2250454	NM_001072.4(UGT1A6):c.862-23551T>C	DNAJB3, UGT1A +8 more	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2238547	NM_001072.4(UGT1A6):c.862-23200A>G	DNAJB3, UGT1A +8 more	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 729124	NM_001072.4(UGT1A6):c.862-23412C>T	DNAJB3, UGT1A +8 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 393977	GRCh37/hg19 2q37.1(chr2:234651441-234652419)x1	DNAJB3, UGT1A10 +7 more	Copy number loss	See cases	GBenign/Likely benign

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