ClinVar Miner

List of variants in gene NDN studied for Prader-Willi syndrome

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_002487.3(NDN):c.212A>G (p.Gln71Arg) rs1891161078
NM_002487.3(NDN):c.472dup (p.Thr158fs) rs1891151702
NM_002487.3(NDN):c.533G>A (p.Arg178Lys) rs1555376130
NM_002487.3(NDN):c.871C>A (p.Pro291Thr) rs2140756886

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