List of variants in gene COL1A2 reported as likely benign by Center for Human Genetics, Inc, Center for Human Genetics, Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000089.4(COL1A2):c.808G>A (p.Val270Ile)	rs368468	0.00177
NM_000089.4(COL1A2):c.2123G>A (p.Arg708Gln)	rs72658163	0.00077
NM_000089.4(COL1A2):c.304C>T (p.Pro102Ser)	rs189557655	0.00060
NM_000089.4(COL1A2):c.2163C>T (p.Gly721=)	rs150670521	0.00025
NM_000089.4(COL1A2):c.2168A>G (p.Asn723Ser)	rs189374343	0.00016
NM_000089.4(COL1A2):c.2836-17C>T	rs370073620	0.00014
NM_000089.4(COL1A2):c.2566-6A>G	rs141088934	0.00012
NM_000089.4(COL1A2):c.48C>T (p.Thr16=)	rs780687409	0.00004
NM_000089.4(COL1A2):c.1251+19dup	rs762359173	0.00001
NM_000089.4(COL1A2):c.1447G>A (p.Ala483Thr)	rs960325497	0.00001
NM_000089.4(COL1A2):c.81+8A>C	rs765118884	0.00001
NM_000089.4(COL1A2):c.96+13T>C	rs1554394649

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