ClinVar Miner

Variants in gene NEXN 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: 8
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HGVS dbSNP
NM_144573.3(NEXN):c.242A>T (p.Asp81Val) rs367871780
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.4(NEXN):c.1252-10T>G rs201019553
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del) rs794729091
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.4(NEXN):c.865-5G>A rs727505353
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg) rs200753280

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