Related gene-specific medical variations for Gene (Select 64927) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808054	GRCh37/hg19 15q26.3(chr15:99722842-99760335)x1	TTC23	Copy number loss	not provided	GUncertain significance
Select item 1340146	GRCh37/hg19 15q26.3(chr15:99722958-99760335)x1	TTC23	Copy number loss	not provided	GUncertain significance
Select item 917963	NM_001288615.3(TTC23):c.456-1G>T	LOC126862246, TTC23	Single nucleotide variant (splice acceptor variant)	Orofaciodigital syndrome	GBenign
Select item 564236	GRCh37/hg19 15q26.3(chr15:99722841-99760335)x1	TTC23	Copy number loss	not provided	GUncertain significance

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