ClinVar for Gene (Select 391322) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2399148	NR_186859.1(LOC391322):n.248A>G	LOC391322	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2384300	NR_186859.1(LOC391322):n.214T>G	LOC391322	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2259098	NR_186859.1(LOC391322):n.50C>T	LOC391322	Single nucleotide variant	Inborn genetic diseases	GUncertain significance
Select item 147980	GRCh37/hg19 22q11.23(chr22:24371005-24382415)x0	GSTT1, GSTT1-AS1 +1 more	Copy number loss	See cases	GBenign
Select item 147167	GRCh37/hg19 22q11.23(chr22:24328565-24385948)x0	GSTT1, GSTT1-AS1 +2 more	Copy number loss	See cases	GBenign
Select item 147012	GRCh37/hg19 22q11.23(chr22:24347988-24385948)x1	GSTT1, GSTT1-AS1 +1 more	Copy number loss	See cases	GBenign

ClinVar