List of variants in gene PLEC reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_201384.3(PLEC):c.7669C>T (p.Arg2557Trp)	rs201569045	0.00054
NM_201384.3(PLEC):c.2719C>T (p.Arg907Cys)	rs201386370	0.00029
NM_201384.3(PLEC):c.4526G>A (p.Arg1509His)	rs782666455	0.00028
NM_201384.3(PLEC):c.5315C>T (p.Ala1772Val)	rs782439290	0.00026
NM_201384.3(PLEC):c.1438C>T (p.Arg480Cys)	rs202172091	0.00025
NM_201384.3(PLEC):c.13247C>T (p.Thr4416Met)	rs201855218	0.00018
NM_201384.3(PLEC):c.8801C>T (p.Thr2934Met)	rs368122904	0.00013
NM_201384.3(PLEC):c.11066C>T (p.Thr3689Met)	rs377252521	0.00012
NM_201384.3(PLEC):c.5248C>T (p.Arg1750Trp)	rs782410213	0.00009
NM_201384.3(PLEC):c.9406G>A (p.Ala3136Thr)	rs200680102	0.00008
NM_201384.3(PLEC):c.8630C>T (p.Thr2877Met)	rs201565643	0.00005
NM_201384.3(PLEC):c.5482C>T (p.Arg1828Trp)	rs1475632975	0.00004
NM_201384.3(PLEC):c.6083C>T (p.Ala2028Val)	rs781895825	0.00004
NM_201384.3(PLEC):c.10802G>A (p.Arg3601Gln)	rs369570610	0.00003
NM_201384.3(PLEC):c.2497C>T (p.Pro833Ser)	rs782532633	0.00003
NM_201384.3(PLEC):c.10741G>A (p.Gly3581Ser)	rs782459958	0.00002
NM_201384.3(PLEC):c.2742C>A (p.Phe914Leu)	rs1826574724	0.00001
NM_201384.3(PLEC):c.4499G>A (p.Arg1500Gln)	rs782344020	0.00001
NM_201384.3(PLEC):c.4889A>G (p.Glu1630Gly)	rs781881685	0.00001
NM_201384.3(PLEC):c.6064C>T (p.Arg2022Trp)	rs781936068	0.00001
NM_201384.3(PLEC):c.9380G>A (p.Arg3127Gln)	rs552993354	0.00001
NM_201384.3(PLEC):c.12367_12369del (p.Glu4123del)	rs782364560
NM_201384.3(PLEC):c.4373G>T (p.Arg1458Leu)	rs782720526

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