ClinVar Miner

List of variants reported as pathogenic for Feingold syndrome by OMIM

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_005378.6(MYCN):c.1145G>A (p.Arg382His) rs121913666
NM_005378.6(MYCN):c.1177C>A (p.Arg393Ser) rs104893647
NM_005378.6(MYCN):c.1178G>A (p.Arg393His) rs104893646
NM_005378.6(MYCN):c.1181G>A (p.Arg394His) rs104893648
NM_005378.6(MYCN):c.217G>T (p.Glu73Ter) rs113994115
NM_005378.6(MYCN):c.231G>A (p.Trp77Ter) rs121913667
NM_005378.6(MYCN):c.626dup (p.Ala210fs) rs1558534266

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