List of variants in gene LAMB1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002291.3(LAMB1):c.3299C>T (p.Thr1100Met)	rs145485632	0.00036
NM_002291.3(LAMB1):c.2458C>T (p.Pro820Ser)	rs140619520	0.00017
NM_002291.3(LAMB1):c.3481C>T (p.Arg1161Cys)	rs146018013	0.00014
NM_002291.3(LAMB1):c.5272G>A (p.Ala1758Thr)	rs201165389	0.00004
NM_002291.3(LAMB1):c.2906T>C (p.Val969Ala)	rs755484957	0.00001
NM_002291.3(LAMB1):c.1033C>T (p.His345Tyr)	rs1064797341
NM_002291.3(LAMB1):c.1562G>C (p.Ser521Thr)
NM_002291.3(LAMB1):c.259G>A (p.Glu87Lys)	rs1262933040
NM_002291.3(LAMB1):c.2609A>G (p.Asn870Ser)	rs564658034
NM_002291.3(LAMB1):c.2951C>T (p.Thr984Met)	rs373568948
NM_002291.3(LAMB1):c.359A>G (p.Asn120Ser)	rs2150453167

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