List of variants in gene PMP22 reported as benign for Hereditary liability to pressure palsies

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000304.4(PMP22):c.*59A>C	rs13422	0.56905
NM_000304.4(PMP22):c.-74A>G	rs114365663	0.01441
NM_000304.4(PMP22):c.-86A>C	rs140650630	0.00832
NM_000304.4(PMP22):c.353C>T (p.Thr118Met)	rs104894619	0.00378
NM_000304.4(PMP22):c.*912G>A	rs149070440	0.00366
NM_000304.4(PMP22):c.403G>A (p.Ala135Thr)	rs141094419	0.00278
NM_000304.4(PMP22):c.178+7C>A	rs147885521	0.00111
NM_000304.4(PMP22):c.79-6C>T	rs201682989	0.00069
NM_000304.4(PMP22):c.*200T>G	rs142106420	0.00063
NM_000304.4(PMP22):c.*173C>T	rs117277951	0.00044
NM_000304.4(PMP22):c.*890C>T	rs546778557	0.00006
NM_000304.4(PMP22):c.*376C>T	rs575964802

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