ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 11
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HGVS dbSNP
NM_002292.4(LAMB2):c.1193C>T (p.Thr398Ile) rs77500937
NM_002292.4(LAMB2):c.1206G>A (p.Arg402=) rs201999373
NM_002292.4(LAMB2):c.1764C>T (p.Pro588=) rs33942096
NM_002292.4(LAMB2):c.2307C>T (p.Leu769=) rs147076626
NM_002292.4(LAMB2):c.2740G>A (p.Gly914Arg) rs35713889
NM_002292.4(LAMB2):c.2959G>A (p.Glu987Lys) rs34759087
NM_002292.4(LAMB2):c.306C>T (p.Asn102=) rs79448908
NM_002292.4(LAMB2):c.3387A>G (p.Gln1129=) rs34290943
NM_002292.4(LAMB2):c.4774C>T (p.Arg1592Trp) rs61729458
NM_002292.4(LAMB2):c.5166A>G (p.Gln1722=) rs114485284
NM_002292.4(LAMB2):c.5293G>A (p.Ala1765Thr) rs74951356

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