ClinVar Miner

List of variants in gene combination LOC126805765, NEXN reported as likely benign for dilated cardiomyopathy

Included ClinVar conditions (248):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_144573.4(NEXN):c.270A>G (p.Val90=) rs756902771 0.00006
NM_144573.4(NEXN):c.299-10A>G rs1452768769 0.00001
NM_144573.4(NEXN):c.299-14T>C rs921990698 0.00001
NM_144573.4(NEXN):c.373C>A (p.Arg125=) rs773500471 0.00001
NM_144573.4(NEXN):c.298+9C>T
NM_144573.4(NEXN):c.321T>A (p.Ala107=) rs1553236762
NM_144573.4(NEXN):c.345G>A (p.Glu115=)
NM_144573.4(NEXN):c.352A>C (p.Arg118=) rs2102094430
NM_144573.4(NEXN):c.378A>G (p.Lys126=)
NM_144573.4(NEXN):c.381C>A (p.Arg127=) rs2102094631
NM_144573.4(NEXN):c.408G>A (p.Lys136=) rs2102094793
NM_144573.4(NEXN):c.447+11A>T

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