List of variants in gene combination C1QTNF5, MFRP reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_031433.4(MFRP):c.1374G>T (p.Leu458Phe)	rs145881139	0.00888
NM_031433.4(MFRP):c.641+9C>T	rs189840088	0.00337
NM_031433.4(MFRP):c.1014C>A (p.Ser338Arg)	rs145319149	0.00126
NM_031433.4(MFRP):c.159T>C (p.Gly53=)	rs372897338	0.00011
NM_031433.4(MFRP):c.1256-4G>A	rs142533439	0.00010
NM_031433.4(MFRP):c.1497G>A (p.Glu499=)	rs375425631	0.00009
NM_031433.4(MFRP):c.158-4G>A	rs560861324	0.00002
NM_001278431.2(C1QTNF5):c.198C>T (p.Gly66=)	rs932268494	0.00001
NM_001278431.2(C1QTNF5):c.306G>A (p.Pro102=)	rs751346951	0.00001
NM_031433.4(MFRP):c.465C>T (p.Phe155=)	rs748084228	0.00001
NM_001278431.2(C1QTNF5):c.354G>A (p.Pro118=)	rs779390261
NM_001278431.2(C1QTNF5):c.583dup (p.Ala195fs)	rs369839371
NM_001278431.2(C1QTNF5):c.648C>T (p.Gly216=)
NM_031433.4(MFRP):c.1164G>T (p.Ser388=)
NM_031433.4(MFRP):c.1458C>T (p.Asn486=)
NM_031433.4(MFRP):c.496C>G (p.Pro166Ala)	rs145285193
NM_031433.4(MFRP):c.657G>T (p.Val219=)
NM_031433.4(MFRP):c.75C>T (p.Ala25=)

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