List of variants in gene COL4A1 reported as not provided

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001845.6(COL4A1):c.922G>A (p.Gly308Arg)	rs370677625	0.00003
NM_001845.6(COL4A1):c.1493G>T (p.Gly498Val)	rs113994104
NM_001845.6(COL4A1):c.1555G>A (p.Gly519Arg)	rs113994105
NM_001845.6(COL4A1):c.1583G>A (p.Gly528Glu)	rs113994106
NM_001845.6(COL4A1):c.1769G>A (p.Gly590Glu)	rs113994107
NM_001845.6(COL4A1):c.1A>T (p.Met1Leu)	rs113994103
NM_001845.6(COL4A1):c.2075C>G (p.Pro692Arg)	rs1566356383
NM_001845.6(COL4A1):c.2159G>A (p.Gly720Asp)	rs113994108
NM_001845.6(COL4A1):c.2245G>A (p.Gly749Ser)	rs113994109
NM_001845.6(COL4A1):c.3389G>A (p.Gly1130Asp)	rs113994111
NM_001845.6(COL4A1):c.3706G>A (p.Gly1236Arg)	rs113994112
NM_001845.6(COL4A1):c.4267G>C (p.Gly1423Arg)	rs113994113
NM_001845.6(COL4A1):c.4738G>C (p.Gly1580Arg)	rs113994114

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