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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000228.3(LAMB3):c.2702-12dup	rs397807887	0.95488
NM_000228.3(LAMB3):c.823-15C>T	rs4844863	0.84219
NM_000228.3(LAMB3):c.1716T>C (p.Cys572=)	rs2179402	0.74805
NM_000228.3(LAMB3):c.291A>C (p.Ser97=)	rs2076356	0.56410
NM_000228.3(LAMB3):c.3432A>G (p.Ser1144=)	rs1049607	0.44327
NM_000228.3(LAMB3):c.384C>T (p.Pro128=)	rs1130667	0.30741
NM_000228.3(LAMB3):c.298+50T>A	rs2076355	0.28812
NM_000228.3(LAMB3):c.138C>T (p.Thr46=)	rs2228339	0.25110
NM_000228.3(LAMB3):c.1579G>A (p.Val527Met)	rs2076349	0.12644
NM_000228.3(LAMB3):c.1486-18G>A	rs2076350	0.12625
NM_000228.3(LAMB3):c.2673A>G (p.Leu891=)	rs3179860	0.11219
NM_000228.3(LAMB3):c.2554A>T (p.Met852Leu)	rs12748250	0.11215
NM_000228.3(LAMB3):c.1149G>A (p.Pro383=)	rs2076351	0.05772
NM_000228.3(LAMB3):c.2777C>A (p.Ala926Asp)	rs2076222	0.02691
NM_000228.3(LAMB3):c.15C>T (p.Phe5=)	rs140470350	0.00190
NM_000228.3(LAMB3):c.2933G>C (p.Gly978Ala)	rs138748613	0.00102
NM_000228.3(LAMB3):c.1188C>T (p.Thr396=)	rs115883756	0.00082
NM_000228.3(LAMB3):c.1258C>G (p.Leu420Val)	rs376412573	0.00003
NM_000228.3(LAMB3):c.822+33G>C	rs2072940

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