List of variants in gene LAMB3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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_000228.3(LAMB3):c.2286C>T (p.Thr762=)	rs11555726	0.00282
NM_000228.3(LAMB3):c.332A>G (p.Asp111Gly)	rs55824996	0.00198
NM_000228.3(LAMB3):c.2147G>A (p.Arg716Gln)	rs114174766	0.00191
NM_000228.3(LAMB3):c.3124C>T (p.Arg1042Trp)	rs114040223	0.00132
NM_000228.3(LAMB3):c.1051G>A (p.Glu351Lys)	rs114875539	0.00107
NM_000228.3(LAMB3):c.1194G>A (p.Gln398=)	rs116602483	0.00103
NM_000228.3(LAMB3):c.1413G>A (p.Lys471=)	rs112316651	0.00096
NM_000228.3(LAMB3):c.2871G>A (p.Ala957=)	rs143164025	0.00022
NM_000228.3(LAMB3):c.1549C>T (p.Arg517Cys)	rs78788119	0.00020
NM_000228.3(LAMB3):c.1616G>A (p.Arg539Gln)	rs530692211	0.00003
NM_000228.3(LAMB3):c.3411C>T (p.Ser1137=)	rs771886651	0.00002
NM_000228.3(LAMB3):c.453C>T (p.Ala151=)	rs369986809	0.00002
NM_000228.3(LAMB3):c.1133-30C>T
NM_000228.3(LAMB3):c.2962C>A (p.Arg988=)	rs2229467
NM_000228.3(LAMB3):c.629-5C>A
NM_000228.3(LAMB3):c.875G>T (p.Arg292Leu)	rs12091253
NM_000228.3(LAMB3):c.927C>T (p.Asp309=)	rs141059189

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