List of variants in gene MTTP reported as likely benign by GeneDx

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001386140.1(MTTP):c.249+23A>G	rs17532601	0.02468
NM_001386140.1(MTTP):c.*113G>C	rs112407688	0.02360
NM_001386140.1(MTTP):c.1981G>A (p.Gly661Ser)	rs113337987	0.02355
NM_001386140.1(MTTP):c.393+234G>A	rs151253743	0.02355
NM_001386140.1(MTTP):c.1345-77C>T	rs112125838	0.02264
NM_001386140.1(MTTP):c.1867+36C>T	rs112568939	0.02260
NM_001386140.1(MTTP):c.660T>C (p.Tyr220=)	rs113557405	0.02258
NM_001386140.1(MTTP):c.*279C>G	rs115807483	0.01703
NM_001386140.1(MTTP):c.758+201A>T	rs113930953	0.01135
NM_001386140.1(MTTP):c.2636A>G (p.Lys879Arg)	rs114049933	0.01021
NM_001386140.1(MTTP):c.502G>A (p.Val168Ile)	rs61750974	0.00790
NM_001386140.1(MTTP):c.*267A>C	rs79992570	0.00645
NM_001386140.1(MTTP):c.1344+99C>T	rs182827300	0.00607
NM_001386140.1(MTTP):c.2342+238A>G	rs140549441	0.00569
NM_001386140.1(MTTP):c.2043G>A (p.Glu681=)	rs145444300	0.00389
NM_001386140.1(MTTP):c.501+62T>C	rs991812	0.00359
NM_001386140.1(MTTP):c.1731C>T (p.Ala577=)	rs112506924	0.00290
NM_001386140.1(MTTP):c.-6G>A	rs41275707	0.00266
NM_001386140.1(MTTP):c.552A>T (p.Lys184Asn)	rs144315111	0.00250
NM_001386140.1(MTTP):c.2673C>T (p.Ser891=)	rs115222767	0.00236
NM_001386140.1(MTTP):c.419A>G (p.Asn140Ser)	rs61733140	0.00162
NM_001386140.1(MTTP):c.2433G>C (p.Leu811Phe)	rs144590904	0.00139
NM_001386140.1(MTTP):c.1068-108dup	rs5860584
NM_001386140.1(MTTP):c.1990-97C>A	rs41275717

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