Related gene-specific medical variations for Gene (Select 677832) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1269840	NM_002635.4(SLC25A3):c.642-109A>G	SLC25A3, SNORA53	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1228798	NM_002635.4(SLC25A3):c.642-90C>T	SLC25A3, SNORA53	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1183192	NM_002635.4(SLC25A3):c.642-145A>G	SLC25A3, SNORA53	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

Format

Sort by

Choose Destination