List of variants in gene LAMB2 reported by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002292.4(LAMB2):c.2740G>A (p.Gly914Arg)	rs35713889	0.03588
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.3858G>T (p.Val1286=)	rs34967349	0.00312
NM_002292.4(LAMB2):c.109C>G (p.Pro37Ala)	rs144765752	0.00242
NM_002292.4(LAMB2):c.598G>A (p.Val200Ile)	rs149325182	0.00034
NM_002292.4(LAMB2):c.1206G>A (p.Arg402=)	rs201999373	0.00012
NM_002292.4(LAMB2):c.3470G>A (p.Arg1157His)	rs766772811	0.00007
NM_002292.4(LAMB2):c.2983A>G (p.Met995Val)	rs773681564	0.00006
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.1599-1G>T	rs1330915067
NM_002292.4(LAMB2):c.3811G>A (p.Glu1271Lys)	rs1560071889
NM_002292.4(LAMB2):c.5061G>T (p.Thr1687=)	rs150465100

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