ClinVar Miner

List of variants reported as pathogenic for Feingold syndrome by GeneReviews

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_005378.6(MYCN):c.1103_1104AG[3] (p.Ser369fs)
NM_005378.6(MYCN):c.1117C>T (p.Arg373Ter) rs754137452
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.964C>T (p.Arg322Ter) rs759103701

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