Related gene-specific medical variations for Gene (Select 164684) - 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 901974	NM_000262.3(NAGA):c.*1930G>A	NAGA, WBP2NL	Single nucleotide variant (3 prime UTR variant)	Alpha-N-acetylgalactosaminidase deficiency type 2 +1 more	GLikely benign
Select item 341885	NM_000262.3(NAGA):c.*1929C>T	NAGA, WBP2NL	Single nucleotide variant (3 prime UTR variant)	Alpha-N-acetylgalactosaminidase deficiency type 2 +1 more	GBenign