ClinVar for MedGen (Select 473805) - ClinVar

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

Format

Sort by

Choose Destination

Links from MedGen

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1710092	NM_002187.3(IL12B):c.89-14T>C	IL12B	Single nucleotide variant (intron variant)	Inherited susceptibility to mycobacterial diseases	GLikely benign
Select item 1710091	NM_004120.5(GBP2):c.1149+14T>C	GBP2	Single nucleotide variant (intron variant)	Inherited susceptibility to mycobacterial diseases	GLikely risk allele