List of variants in gene MPZ reported as benign for not provided

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000530.8(MPZ):c.448+64T>C	rs6674383	1.00000
NM_000530.6(MPZ):c.-187T>C	rs28703151	0.38691
NM_000530.8(MPZ):c.448+122C>T	rs6685495	0.22833
NM_000530.8(MPZ):c.67+272C>A	rs376976260	0.17827
NM_000530.8(MPZ):c.*761A>G	rs16832786	0.13087
NC_000001.11:g.161304658G>C	rs71639056	0.09209
NM_000530.8(MPZ):c.67+111A>G	rs11579939	0.07848
NM_000530.8(MPZ):c.67+287del	rs200584940	0.04675
NM_000530.8(MPZ):c.684C>T (p.Ser228=)	rs34307129	0.01960
NM_000530.8(MPZ):c.*624C>T	rs60821801	0.01537
NM_000530.8(MPZ):c.*195G>T	rs150182811	0.00828
NM_000530.8(MPZ):c.*1048A>T	rs71639057	0.00663
NM_000530.8(MPZ):c.646-29G>C	rs61458643	0.00362
NM_000530.8(MPZ):c.51G>A (p.Leu17=)	rs149637045	0.00019
NM_000530.8(MPZ):c.*901GA[7]	rs149030537

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