List of variants reported as pathogenic for Feingold syndrome type 1 by OMIM

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
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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