Related gene-specific medical variations for Gene (Select 100287290) - 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 3151658	NM_206963.2(RARRES1):c.34T>C (p.Trp12Arg)	LOC100287290, RARRES1 (W12R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2344505	NM_206963.2(RARRES1):c.34T>A (p.Trp12Arg)	LOC100287290, RARRES1 (W12R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign