ClinVar Miner

List of variants studied for Feingold syndrome by GeneReviews

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_005378.6(MYCN):c.-211C>T rs887665529 0.00001
NM_005378.6(MYCN):c.1105_1106dup (p.Ser369fs) rs1572221400
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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