List of variants in gene LAMC3 reported as uncertain significance by Baylor 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.4160C>T (p.Ala1387Val)	rs141497885	0.00258
NM_006059.4(LAMC3):c.4424G>A (p.Arg1475His)	rs113354770	0.00033
NM_006059.4(LAMC3):c.1066C>T (p.Arg356Cys)	rs138713603	0.00030
NM_006059.4(LAMC3):c.4415G>A (p.Arg1472Gln)	rs137894550	0.00029
NM_006059.4(LAMC3):c.1185C>T (p.Cys395=)	rs186634083	0.00018
NM_006059.4(LAMC3):c.4414C>T (p.Arg1472Trp)	rs145848963	0.00015
NM_006059.4(LAMC3):c.1611G>C (p.Glu537Asp)	rs772723882	0.00006
NM_006059.4(LAMC3):c.4523C>T (p.Thr1508Ile)	rs1186517778	0.00006
NM_006059.4(LAMC3):c.557G>A (p.Arg186His)	rs145176060	0.00001
NM_006059.4(LAMC3):c.2950G>C (p.Val984Leu)	rs527388604
NM_006059.4(LAMC3):c.4198G>A (p.Glu1400Lys)	rs1830319465

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