"PreventionGenetics, part of Exact Sciences"[submitter] AND "CXCL12"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1233193	NM_001277990.2(CXCL12):c.183G>A (p.Leu61=)	CXCL12	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 3037442	NM_001277990.2(CXCL12):c.110-6A>G	CXCL12	Single nucleotide variant (3 prime UTR variant +1 more)	CXCL12-related condition	GLikely benign
Select item 3044678	NM_199168.4(CXCL12):c.*884A>G	CXCL12	Single nucleotide variant (intron variant +2 more)	CXCL12-related condition	GLikely benign
Select item 2640421	NM_199168.4(CXCL12):c.*881G>T	CXCL12	Single nucleotide variant (synonymous variant +2 more)	CXCL12-related condition +1 more	GBenign/Likely benign
Select item 3058031	NM_199168.4(CXCL12):c.*749C>T	CXCL12	Single nucleotide variant (synonymous variant +2 more)	CXCL12-related condition	GLikely benign
Select item 3056613	NM_199168.4(CXCL12):c.-27CCGC[5]	CXCL12	Microsatellite (5 prime UTR variant)	CXCL12-related condition	GBenign

ClinVar