List of variants in gene LAMB2 reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_002292.4(LAMB2):c.1306G>A (p.Gly436Ser)	rs142402808	0.00096
NM_002292.4(LAMB2):c.703C>T (p.Arg235Trp)	rs144133177	0.00071
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.4001G>C (p.Arg1334Pro)	rs144783830	0.00004
NM_002292.4(LAMB2):c.2219G>A (p.Arg740His)	rs781721930	0.00003

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