List of variants in gene LAMC2 reported as likely pathogenic by Invitae

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_005562.3(LAMC2):c.1468+1G>T	rs1043996591	0.00003
NM_005562.3(LAMC2):c.80-2A>G	rs771613805	0.00002
NM_005562.3(LAMC2):c.1715-2A>G	rs769983361	0.00001
NM_005562.3(LAMC2):c.954-1G>A	rs149195906	0.00001
NC_000001.10:g.(?_183196339)_(183197630_?)del
NC_000001.10:g.(?_183197499)_(183206649_?)dup
NC_000001.10:g.(?_183204785)_(183204878_?)del
NM_005562.3(LAMC2):c.1285+1G>A	rs2102230520
NM_005562.3(LAMC2):c.1715-1G>C	rs774080932
NM_005562.3(LAMC2):c.2015-1G>T	rs2102239920
NM_005562.3(LAMC2):c.2220+2T>C
NM_005562.3(LAMC2):c.2601+1G>C
NM_005562.3(LAMC2):c.2602-1G>A	rs1553267499
NM_005562.3(LAMC2):c.268+1G>A	rs759509443
NM_005562.3(LAMC2):c.269-1G>T
NM_005562.3(LAMC2):c.3069+1G>A
NM_005562.3(LAMC2):c.3229-1G>A
NM_005562.3(LAMC2):c.503+1G>C	rs1057516410
NM_005562.3(LAMC2):c.504-51_550del	rs2102219621
NM_005562.3(LAMC2):c.640+1G>A	rs1183519794
NM_005562.3(LAMC2):c.764-1G>A
NM_005562.3(LAMC2):c.80-2A>C	rs771613805

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