List of variants in gene PPM1D reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_003620.4(PPM1D):c.1017+3929A>C	rs143487178	0.01201
NM_003620.4(PPM1D):c.472+1152A>G	rs79979798	0.00413
NM_003620.4(PPM1D):c.472+314G>A	rs570481796	0.00350
NM_003620.4(PPM1D):c.702-21A>G	rs138641521	0.00337
NM_003620.4(PPM1D):c.1017+51A>G	rs144142345	0.00301
NM_003620.4(PPM1D):c.702-2064T>C	rs112711419	0.00301
NM_003620.4(PPM1D):c.701+366C>T	rs528453003	0.00136
NM_003620.4(PPM1D):c.473-1294T>C	rs148672464	0.00109
NM_003620.4(PPM1D):c.701+3346A>G	rs869312627	0.00001
NM_003620.4(PPM1D):c.1260+2807G>A	rs869312625
NM_003620.4(PPM1D):c.1261-1386A>G	rs869312626
NM_003620.4(PPM1D):c.472+4585C>T	rs869312630
NM_003620.4(PPM1D):c.472+77G>A	rs869312628
NM_003620.4(PPM1D):c.702-3299C>T	rs869312629

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