List of variants in gene LAMB1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002291.3(LAMB1):c.3012G>A (p.Thr1004=)	rs113725211	0.00487
NM_002291.3(LAMB1):c.4221C>T (p.Ser1407=)	rs35082294	0.00416
NM_002291.3(LAMB1):c.2542G>C (p.Ala848Pro)	rs145746791	0.00371
NM_002291.3(LAMB1):c.1590A>C (p.Ser530=)	rs139481973	0.00175
NM_002291.3(LAMB1):c.2691-9C>T	rs751631641	0.00044
NM_002291.3(LAMB1):c.3642G>T (p.Gly1214=)	rs569355700	0.00021
NM_002291.3(LAMB1):c.3834C>T (p.Ser1278=)	rs1389549765	0.00002
NM_002291.3(LAMB1):c.1944C>T (p.Pro648=)	rs751175194	0.00001

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