List of variants in gene LAMB2 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_002292.4(LAMB2):c.3858G>T (p.Val1286=)	rs34967349	0.00312
NM_002292.4(LAMB2):c.510C>T (p.Arg170=)	rs149856537	0.00167
NM_002292.4(LAMB2):c.5061G>A (p.Thr1687=)	rs150465100	0.00025
NM_002292.4(LAMB2):c.915+16C>T	rs376022767	0.00025
NM_002292.4(LAMB2):c.460-8C>G	rs200141829	0.00018
NM_002292.4(LAMB2):c.2344+14A>T	rs369733428	0.00016
NM_002292.4(LAMB2):c.4257T>C (p.Ala1419=)	rs149536828	0.00016
NM_002292.4(LAMB2):c.2720+11A>G	rs370034592	0.00012
NM_002292.4(LAMB2):c.4425C>T (p.Ser1475=)	rs140142444	0.00011
NM_002292.4(LAMB2):c.1422A>C (p.Ala474=)	rs201408584	0.00006
NM_002292.4(LAMB2):c.1890+19A>C	rs763388406	0.00006
NM_002292.4(LAMB2):c.4071T>C (p.Pro1357=)	rs770830943	0.00006
NM_002292.4(LAMB2):c.3826C>T (p.Leu1276=)	rs754393937	0.00004
NM_002292.4(LAMB2):c.1383C>T (p.Ile461=)	rs373952285	0.00003
NM_002292.4(LAMB2):c.4305G>A (p.Pro1435=)	rs371257983	0.00003
NM_002292.4(LAMB2):c.4863C>G (p.Ala1621=)	rs753340192	0.00003
NM_002292.4(LAMB2):c.1074C>T (p.Phe358=)	rs765736533	0.00001
NM_002292.4(LAMB2):c.1329T>C (p.His443=)	rs1131787	0.00001
NM_002292.4(LAMB2):c.1392T>A (p.Arg464=)	rs922993666	0.00001
NM_002292.4(LAMB2):c.1519-5T>C	rs1242908578	0.00001
NM_002292.4(LAMB2):c.252C>T (p.Asp84=)	rs750432118	0.00001
NM_002292.4(LAMB2):c.3798-17C>G	rs777266280	0.00001
NM_002292.4(LAMB2):c.4848G>A (p.Arg1616=)	rs567190427	0.00001
NM_002292.4(LAMB2):c.951T>A (p.Arg317=)	rs755050242	0.00001
NM_002292.4(LAMB2):c.1519-6G>A	rs755545118
NM_002292.4(LAMB2):c.1683G>T (p.Arg561=)	rs760427008
NM_002292.4(LAMB2):c.3798-16del	rs750912455
NM_002292.4(LAMB2):c.5061G>T (p.Thr1687=)	rs150465100
NM_002292.4(LAMB2):c.762G>A (p.Thr254=)	rs201406827

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