List of variants in gene combination COL4A3, MFF-DT reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.4510T>C (p.Phe1504Leu)	rs201671013	0.00024
NM_000091.5(COL4A3):c.4523A>G (p.Asn1508Ser)	rs200512461	0.00022
NM_000091.5(COL4A3):c.206A>C (p.Glu69Ala)	rs755344973	0.00002
NM_000091.5(COL4A3):c.361G>A (p.Gly121Ser)	rs778886174	0.00001
NM_000091.5(COL4A3):c.3251A>T (p.Glu1084Val)	rs2072858880
NM_000091.5(COL4A3):c.4673T>C (p.Ile1558Thr)	rs2073643599
NM_000091.5(COL4A3):c.568T>A (p.Phe190Ile)	rs371173786

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