List of variants in gene LAMC3 reported as uncertain significance 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.4092C>T (p.Ser1364=)	rs141724499	0.00360
NM_006059.4(LAMC3):c.2891-8C>T	rs199535979	0.00339
NM_006059.4(LAMC3):c.2517G>A (p.Thr839=)	rs140540789	0.00292
NM_006059.4(LAMC3):c.4160C>T (p.Ala1387Val)	rs141497885	0.00258
NM_006059.4(LAMC3):c.1520-6G>A	rs192031352	0.00175
NM_006059.4(LAMC3):c.2066C>T (p.Pro689Leu)	rs113443891	0.00123
NM_006059.4(LAMC3):c.3409G>C (p.Ala1137Pro)	rs149766298	0.00041
NM_006059.4(LAMC3):c.1019G>A (p.Arg340Gln)	rs149004188	0.00037
NM_006059.4(LAMC3):c.3607A>T (p.Thr1203Ser)	rs141639990	0.00006
NM_006059.4(LAMC3):c.4031-10G>A	rs555619019	0.00001
NM_006059.4(LAMC3):c.4698C>T (p.Ser1566=)	rs754122699	0.00001
NM_006059.4(LAMC3):c.4705G>A (p.Glu1569Lys)	rs145287578	0.00001
NM_006059.4(LAMC3):c.1939G>C (p.Gly647Arg)	rs144242690
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln)	rs146221263
NM_006059.4(LAMC3):c.3379G>A (p.Glu1127Lys)	rs140955110
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser)	rs147092908
NM_006059.4(LAMC3):c.422G>A (p.Arg141His)	rs756873191

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