List of variants in gene PITPNM3 reported as benign by Eurofins NTD LLC (GA)

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_031220.4(PITPNM3):c.705C>T (p.Thr235=)	rs938288	0.50749
NM_031220.4(PITPNM3):c.1625-9G>A	rs11654175	0.36838
NM_031220.4(PITPNM3):c.1773+19C>T	rs9913373	0.04671
NM_031220.4(PITPNM3):c.901-10G>C	rs77580616	0.00927
NM_031220.4(PITPNM3):c.541G>A (p.Val181Ile)	rs61755430	0.00628
NM_031220.4(PITPNM3):c.432C>T (p.Ala144=)	rs149039090	0.00313
NM_031220.4(PITPNM3):c.226+9C>G	rs145880642	0.00273
NM_031220.4(PITPNM3):c.2620-34CCTGCCCTCC[2]	rs759362748

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