Related gene-specific medical variations for Gene (Select 106736613) - ClinVar - NCBI

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

Links from Gene

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053801	NM_020975.6(RET):c.73+9398G>A	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	RET-related condition	GLikely benign
Select item 3048275	NM_020975.6(RET):c.73+9405G>A	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	RET-related condition	GLikely benign
Select item 3036896	NM_020975.6(RET):c.73+9408A>G	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	RET-related condition	GLikely benign
Select item 3029773	NM_020975.6(RET):c.73+9390C>T	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	RET-related condition	GLikely benign
Select item 1290350	NM_020975.6(RET):c.73+9189C>A	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254248	NM_020975.6(RET):c.73+9189C>T	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1229701	NM_020975.6(RET):c.73+9331A>G	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1189903	NM_020975.6(RET):c.73+9385_73+9395del	LOC110121502, MCS+9.7 +1 more	Deletion (intron variant)	Multiple endocrine neoplasia, type 2 +2 more	GBenign/Likely benign
Select item 695195	NM_020975.6(RET):c.73+9494A>C	RET, LOC110121502 +1 more	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 378478	NM_020975.6(RET):c.73+9201C>T	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 372083	NM_020975.6(RET):c.73+9278G>A	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB +1 more	GLikely benign
Select item 13952	NM_020975.6(RET):c.73+9277T>C	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not specified +2 more	GBenign; risk factor