ClinVar Miner

List of variants reported as benign for Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003620.4(PPM1D):c.456C>T (p.Ala152=)	rs149400522	0.00471
NM_003620.4(PPM1D):c.1017+51A>G	rs144142345	0.00298
NM_003620.4(PPM1D):c.1262C>A (p.Ser421Ter)	rs2031551111

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