List of variants reported as uncertain significance for Van Maldergem syndrome 1 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003737.4(DCHS1):c.704G>A (p.Arg235Gln)	rs143767864	0.00077
NM_003737.4(DCHS1):c.644G>A (p.Arg215Gln)	rs529671660	0.00003
NM_003737.4(DCHS1):c.8848G>C (p.Val2950Leu)	rs1403716331	0.00001
NM_003737.4(DCHS1):c.395G>A (p.Arg132Gln)	rs771891400
NM_003737.4(DCHS1):c.5552A>G (p.His1851Arg)	rs759281674

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