List of variants in gene PITPNM3 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_031220.4(PITPNM3):c.699C>T (p.Val233=)	rs149964592	0.00707
NM_031220.4(PITPNM3):c.541G>A (p.Val181Ile)	rs61755430	0.00628
NM_031220.4(PITPNM3):c.2472G>A (p.Leu824=)	rs144737056	0.00305
NM_031220.4(PITPNM3):c.*2281AG[4]
NM_031220.4(PITPNM3):c.*2316GA[6]
NM_031220.4(PITPNM3):c.*2381AG[5]	rs553650590
NM_031220.4(PITPNM3):c.*3454G>C

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