ClinVar Miner

Variants in gene LAMB2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 9
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HGVS dbSNP
NM_002292.4(LAMB2):c.1206G>A (p.Arg402=) rs201999373
NM_002292.4(LAMB2):c.2152C>T (p.Leu718=) rs756535650
NM_002292.4(LAMB2):c.2922G>C (p.Gly974=) rs145465720
NM_002292.4(LAMB2):c.3582C>T (p.Phe1194=) rs138540017
NM_002292.4(LAMB2):c.4878G>A (p.Arg1626=) rs148648480
NM_002292.4(LAMB2):c.5026G>A (p.Gly1676Arg) rs200747448
NM_002292.4(LAMB2):c.5027G>T (p.Gly1676Val) rs199580679
NM_002292.4(LAMB2):c.5109C>T (p.Arg1703=) rs151292828
NM_002292.4(LAMB2):c.816T>C (p.Tyr272=) rs151251039

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