List of variants in gene LAMB2 reported as benign by Invitae

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_002292.4(LAMB2):c.2959G>A (p.Glu987Lys)	rs34759087	0.09080
NM_002292.4(LAMB2):c.3387A>G (p.Gln1129=)	rs34290943	0.09068
NM_002292.4(LAMB2):c.2740G>A (p.Gly914Arg)	rs35713889	0.03588
NM_002292.4(LAMB2):c.306C>T (p.Asn102=)	rs79448908	0.02014
NM_002292.4(LAMB2):c.5293G>A (p.Ala1765Thr)	rs74951356	0.01940
NM_002292.4(LAMB2):c.1764C>T (p.Pro588=)	rs33942096	0.01677
NM_002292.4(LAMB2):c.4923+17A>G	rs116836607	0.01580
NM_002292.4(LAMB2):c.1724G>A (p.Arg575Gln)	rs61729152	0.01347
NM_002292.4(LAMB2):c.4774C>T (p.Arg1592Trp)	rs61729458	0.01273
NM_002292.4(LAMB2):c.1193C>T (p.Thr398Ile)	rs77500937	0.00775
NM_002292.4(LAMB2):c.2673C>T (p.Gly891=)	rs144092322	0.00741
NM_002292.4(LAMB2):c.3443G>A (p.Arg1148His)	rs138774635	0.00663
NM_002292.4(LAMB2):c.4222C>T (p.Leu1408=)	rs143974640	0.00662
NM_002292.4(LAMB2):c.3110-15T>C	rs147446447	0.00622
NM_002292.4(LAMB2):c.4034G>A (p.Arg1345His)	rs75073433	0.00463
NM_002292.4(LAMB2):c.3858G>T (p.Val1286=)	rs34967349	0.00312
NM_002292.4(LAMB2):c.2307C>T (p.Leu769=)	rs147076626	0.00235
NM_002292.4(LAMB2):c.5166A>G (p.Gln1722=)	rs114485284	0.00173
NM_002292.4(LAMB2):c.510C>T (p.Arg170=)	rs149856537	0.00167
NM_002292.4(LAMB2):c.4163G>A (p.Arg1388Gln)	rs146522641	0.00159
NM_002292.4(LAMB2):c.3645G>A (p.Ala1215=)	rs13082063	0.00137
NM_002292.4(LAMB2):c.3325G>A (p.Glu1109Lys)	rs79677861	0.00036
NM_002292.4(LAMB2):c.1305C>T (p.Ser435=)	rs144530798	0.00034
NM_002292.4(LAMB2):c.4928A>G (p.Gln1643Arg)	rs201844235	0.00031
NM_002292.4(LAMB2):c.2095G>C (p.Gly699Arg)	rs28364667	0.00030
NM_002292.4(LAMB2):c.4370G>A (p.Arg1457Gln)	rs148818522	0.00029
NM_002292.4(LAMB2):c.101C>A (p.Ala34Asp)	rs202057459	0.00024
NM_002292.4(LAMB2):c.4878G>A (p.Arg1626=)	rs148648480	0.00016
NM_002292.4(LAMB2):c.1226-5G>A	rs545564814	0.00006
NM_002292.4(LAMB2):c.2099G>A (p.Gly700Glu)	rs142860588	0.00006
NM_002292.4(LAMB2):c.3498A>G (p.Pro1166=)	rs186771094	0.00006
NM_002292.4(LAMB2):c.250-14C>T	rs371403310	0.00002
NM_002292.4(LAMB2):c.5026G>A (p.Gly1676Arg)	rs200747448	0.00002
NM_002292.4(LAMB2):c.5027G>T (p.Gly1676Val)	rs199580679	0.00002
NM_002292.4(LAMB2):c.2669C>T (p.Thr890Ile)	rs527639885	0.00001
NM_002292.4(LAMB2):c.3071C>T (p.Pro1024Leu)	rs368506627	0.00001
NM_002292.4(LAMB2):c.4848G>A (p.Arg1616=)	rs567190427	0.00001
NM_002292.4(LAMB2):c.1731+16del	rs766983720
NM_002292.4(LAMB2):c.261G>A (p.Lys87=)	rs149408554
NM_002292.4(LAMB2):c.3152C>T (p.Pro1051Leu)
NM_002292.4(LAMB2):c.3798-16del	rs750912455
NM_002292.4(LAMB2):c.4224+19G>A	rs114913744
NM_002292.4(LAMB2):c.5026_5027delinsAT (p.Gly1676Ile)	rs1575526216
NM_002292.4(LAMB2):c.5061G>T (p.Thr1687=)	rs150465100

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