List of variants in gene PITPNM3 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_031220.4(PITPNM3):c.2156+20C>T	rs75323938	0.00994
NM_031220.4(PITPNM3):c.1086-78C>G	rs62061056	0.00992
NM_031220.4(PITPNM3):c.2472G>A (p.Leu824=)	rs144737056	0.00305
NM_031220.4(PITPNM3):c.1878G>C (p.Gln626His)	rs76024428	0.00212
NM_031220.4(PITPNM3):c.901-34C>A	rs187900964

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