ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) 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.3071C>T (p.Pro1024Leu) rs368506627
NM_002292.4(LAMB2):c.3325G>A (p.Glu1109Lys) rs79677861
NM_002292.4(LAMB2):c.4034G>A (p.Arg1345His) rs75073433
NM_002292.4(LAMB2):c.4222C>T (p.Leu1408=) rs143974640
NM_002292.4(LAMB2):c.4370G>A (p.Arg1457Gln) rs148818522
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

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