List of variants in gene LAMC3 reported as likely pathogenic

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.3871C>T (p.Arg1291Ter)	rs201793200	0.00006
NM_006059.4(LAMC3):c.2593+1G>A	rs141896314	0.00004
NM_006059.4(LAMC3):c.976+1G>C	rs201519274	0.00003
NM_006059.4(LAMC3):c.2594-2A>G	rs778619122	0.00001
NC_000009.11:g.(?_133907412)_(133907582_?)dup
NM_006059.4(LAMC3):c.1128_1165+33del
NM_006059.4(LAMC3):c.1166-1G>A
NM_006059.4(LAMC3):c.1283+1G>A
NM_006059.4(LAMC3):c.1283+1G>C
NM_006059.4(LAMC3):c.1383-1G>A	rs768710385
NM_006059.4(LAMC3):c.2348-1G>C	rs1829945601
NM_006059.4(LAMC3):c.2479_2480del (p.Leu827fs)	rs781432366
NM_006059.4(LAMC3):c.2593+2T>A
NM_006059.4(LAMC3):c.2594-5_2668del
NM_006059.4(LAMC3):c.2819del (p.Pro940fs)	rs1170064033
NM_006059.4(LAMC3):c.2833del (p.Gln945fs)	rs1554789398
NM_006059.4(LAMC3):c.2890+1G>A
NM_006059.4(LAMC3):c.3181del (p.Asp1061fs)	rs1554789671
NM_006059.4(LAMC3):c.3211+1G>A
NM_006059.4(LAMC3):c.3211+2T>C	rs2133322852
NM_006059.4(LAMC3):c.3494+1G>T
NM_006059.4(LAMC3):c.3629+1G>A
NM_006059.4(LAMC3):c.3630-2A>G
NM_006059.4(LAMC3):c.374-2_374-1delinsCC
NM_006059.4(LAMC3):c.4354C>T (p.Gln1452Ter)	rs1588171883
NM_006059.4(LAMC3):c.63del (p.Met22fs)
NM_006059.4(LAMC3):c.694del (p.Thr232fs)
NM_006059.4(LAMC3):c.809+2T>G	rs1564368059
NM_006059.4(LAMC3):c.809+2_809+8del	rs775851709
NM_006059.4(LAMC3):c.903_904del (p.Cys301_Glu302delinsTer)	rs761516738
NM_006059.4(LAMC3):c.976+1G>A	rs201519274
NM_006059.4(LAMC3):c.977-2A>T

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