Related gene-specific medical variations for Gene (Select 101928649) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328818	NM_001346048.2(TRIM52):c.814-629A>G	CTC-338M12.4, TRIM52 (K274E)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2589112	NM_001346048.2(TRIM52):c.814-613T>C	CTC-338M12.4, TRIM52 (L279P)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign