C4225235[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1217331	NM_001368882.1(COL13A1):c.258G>A (p.Thr86=)	COL13A1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1217332	NM_001368882.1(COL13A1):c.463-4G>A	COL13A1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 1217333	NM_001368882.1(COL13A1):c.514-4del	COL13A1	Deletion (intron variant)	not provided +1 more	GBenign
Select item 1217334	NM_001368882.1(COL13A1):c.525A>C (p.Gly175=)	COL13A1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1217335	NM_001368882.1(COL13A1):c.685-1181A>G	COL13A1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1217336	NM_001368882.1(COL13A1):c.744G>A (p.Thr248=)	COL13A1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1217337	NM_001368882.1(COL13A1):c.984C>G (p.Ala328=)	COL13A1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1217338	NM_001368882.1(COL13A1):c.1330-3C>T	COL13A1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar