List of variants in gene LAMB2 reported 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
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
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.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.2307C>T (p.Leu769=)	rs147076626	0.00235
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.1306G>A (p.Gly436Ser)	rs142402808	0.00096
NM_002292.4(LAMB2):c.4118A>G (p.Asp1373Gly)	rs112933248	0.00076
NM_002292.4(LAMB2):c.703C>T (p.Arg235Trp)	rs144133177	0.00071
NM_002292.4(LAMB2):c.3582C>T (p.Phe1194=)	rs138540017	0.00068
NM_002292.4(LAMB2):c.1305C>T (p.Ser435=)	rs144530798	0.00034
NM_002292.4(LAMB2):c.1931G>A (p.Arg644His)	rs200738080	0.00025
NM_002292.4(LAMB2):c.5061G>A (p.Thr1687=)	rs150465100	0.00025
NM_002292.4(LAMB2):c.2271C>A (p.Ser757Arg)	rs143405268	0.00021
NM_002292.4(LAMB2):c.5379C>G (p.Ile1793Met)	rs11550620	0.00019
NM_002292.4(LAMB2):c.1442G>A (p.Ser481Asn)	rs144230655	0.00012
NM_002292.4(LAMB2):c.2167C>T (p.Arg723Cys)	rs145660751	0.00010
NM_002292.4(LAMB2):c.2639A>G (p.Asn880Ser)	rs781619412	0.00009
NM_002292.4(LAMB2):c.1572C>T (p.Cys524=)	rs111883392	0.00004
NM_002292.4(LAMB2):c.4001G>C (p.Arg1334Pro)	rs144783830	0.00004
NM_002292.4(LAMB2):c.2219G>A (p.Arg740His)	rs781721930	0.00003
NM_002292.4(LAMB2):c.4305G>A (p.Pro1435=)	rs371257983	0.00003
NM_002292.4(LAMB2):c.2172C>T (p.Val724=)	rs1426174191
NM_002292.4(LAMB2):c.283C>T (p.Arg95Cys)
NM_002292.4(LAMB2):c.5260+1G>T

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