Related gene-specific medical variations for Gene (Select 8514) - 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 760234	NM_001199862.2(KCNAB2):c.263-6T>C	KCNAB2, LOC126805596	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 736636	NM_001199862.2(KCNAB2):c.263-7C>T	KCNAB2, LOC126805596	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 716038	NM_001199862.2(KCNAB2):c.279C>T (p.Phe93=)	KCNAB2, LOC126805596	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

Format

Sort by

Choose Destination