Related gene-specific medical variations for Gene (Select 23308) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3248200	NC_000021.8:g.(?_45655135)_(45655465_?)del	ICOSLG	Deletion	not provided	GUncertain significance
Select item 1973674	NM_015259.6(ICOSLG):c.14+7C>T	ICOSLG, LOC128462416	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1898088	NM_015259.6(ICOSLG):c.14+16A>C	ICOSLG, LOC128462416	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1636531	NM_015259.6(ICOSLG):c.14+10G>A	ICOSLG, LOC128462416	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1558413	NM_015259.6(ICOSLG):c.14+8G>A	ICOSLG, LOC128462416	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1547967	NM_015259.6(ICOSLG):c.14+19G>A	ICOSLG, LOC128462416	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1542183	NM_015259.6(ICOSLG):c.4C>A (p.Arg2=)	ICOSLG, LOC128462416	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

ClinVar