Variants in gene combination COL4A3, MFF-DT with conflicting interpretations reported as "uncertain significance and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 18

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.4981C>T (p.Arg1661Cys)	rs201697532	0.00039
NM_000091.5(COL4A3):c.1096G>A (p.Gly366Arg)	rs539765620	0.00005
NM_000091.5(COL4A3):c.1450G>A (p.Gly484Arg)	rs777401300	0.00003
NM_000091.5(COL4A3):c.1372G>C (p.Gly458Arg)	rs757341933	0.00002
NM_000091.5(COL4A3):c.2954G>T (p.Gly985Val)	rs121912827	0.00002
NM_000091.5(COL4A3):c.898G>A (p.Gly300Arg)	rs772708743	0.00002
NM_000091.5(COL4A3):c.1372G>A (p.Gly458Arg)	rs757341933	0.00001
NM_000091.5(COL4A3):c.343G>A (p.Gly115Arg)	rs202147112	0.00001
NM_000091.5(COL4A3):c.520G>A (p.Gly174Arg)	rs1014839148	0.00001
NM_000091.5(COL4A3):c.765G>A (p.Thr255=)	rs869025328	0.00001
NM_000091.5(COL4A3):c.1831G>A (p.Gly611Arg)	rs1574753929
NM_000091.5(COL4A3):c.1985G>A (p.Gly662Glu)
NM_000091.5(COL4A3):c.2507G>A (p.Gly836Glu)	rs2072040353
NM_000091.5(COL4A3):c.2990G>A (p.Gly997Glu)	rs1553762113
NM_000091.5(COL4A3):c.3312AAGTCCTGG[1] (p.1105SPG[1])	rs756539994
NM_000091.5(COL4A3):c.3546_3548dup (p.Gly1183dup)	rs1175052474
NM_000091.5(COL4A3):c.4337_4338del (p.Phe1446fs)	rs776244020
NM_000091.5(COL4A3):c.4664C>T (p.Ala1555Val)	rs369575989

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