List of variants in gene COL6A2 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001849.4(COL6A2):c.2160C>G (p.Arg720=)	rs61735829	0.01898
NM_001849.4(COL6A2):c.316G>A (p.Glu106Lys)	rs141703710	0.00717
NM_058174.3(COL6A2):c.2649C>T (p.Phe883=)	rs149172490	0.00540
NM_001849.4(COL6A2):c.510C>T (p.Cys170=)	rs142328765	0.00343
NM_001849.4(COL6A2):c.2558G>A (p.Arg853Gln)	rs144830948	0.00148
NM_001849.4(COL6A2):c.169G>A (p.Val57Ile)	rs768434256	0.00003
NM_001849.4(COL6A2):c.3029T>G (p.Phe1010Cys)	rs1051148162	0.00001
NM_001849.4(COL6A2):c.1070C>T (p.Pro357Leu)	rs199929757
NM_001849.4(COL6A2):c.1251C>T (p.Arg417=)	rs61735827
NM_001849.4(COL6A2):c.2251G>A (p.Asp751Asn)	rs375884809

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