Variants in gene combination C1QTNF5, MFRP with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_031433.4(MFRP):c.540T>C (p.His180=)	rs2510143	0.91859
NM_031433.4(MFRP):c.-88C>T	rs883245	0.49359
NM_031433.4(MFRP):c.406G>A (p.Val136Met)	rs3814762	0.24523
NM_031433.4(MFRP):c.492C>T (p.Tyr164=)	rs36015759	0.23503
NM_031433.4(MFRP):c.1387+3G>A	rs11217241	0.08734
NM_031433.4(MFRP):c.954G>A (p.Leu318=)	rs35885438	0.04136
NM_031433.4(MFRP):c.770G>A (p.Arg257His)	rs61736238	0.03023
NM_031433.4(MFRP):c.355A>G (p.Ile119Val)	rs4639950	0.01611
NM_031433.4(MFRP):c.1374G>T (p.Leu458Phe)	rs145881139	0.00888
NM_031433.4(MFRP):c.1635G>A (p.Ala545=)	rs138370910	0.00631
NM_031433.4(MFRP):c.629G>T (p.Gly210Val)	rs150902999	0.00344
NM_031433.4(MFRP):c.641+9C>T	rs189840088	0.00337
NM_031433.4(MFRP):c.669G>A (p.Thr223=)	rs139222274	0.00187
NM_031433.4(MFRP):c.773-9C>T	rs187321874	0.00176
NM_001278431.2(C1QTNF5):c.294C>T (p.Cys98=)	rs540768941	0.00001
NM_001278431.2(C1QTNF5):c.583dup (p.Ala195fs)	rs369839371

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