List of variants in gene PPIP5K2 reported as benign by GeneDx

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001276277.3(PPIP5K2):c.1738-99A>G	rs257292	0.40408
NM_001276277.3(PPIP5K2):c.907-234G>C	rs27970	0.31962
NM_001276277.3(PPIP5K2):c.2923-140A>G	rs26822	0.24717
NM_001276277.3(PPIP5K2):c.-284-87G>C	rs26525	0.24390
NM_001276277.3(PPIP5K2):c.*44A>G	rs28025	0.24200
NM_001276277.3(PPIP5K2):c.1130+118T>C	rs27896	0.23704
NM_001276277.3(PPIP5K2):c.1404-111A>G	rs34768	0.23446
NM_001276277.3(PPIP5K2):c.1294-17A>G	rs58392548	0.05627
NM_001276277.3(PPIP5K2):c.2754+102T>C	rs79968831	0.05495
NM_001276277.3(PPIP5K2):c.401+34A>G	rs74429703	0.05261
NM_001276277.3(PPIP5K2):c.643-35G>A	rs77582921	0.05174
NM_001276277.3(PPIP5K2):c.1921-49G>C	rs78771956	0.04598
NM_001276277.3(PPIP5K2):c.2062+40T>C	rs59260940	0.04270
NM_001276277.3(PPIP5K2):c.1029-169G>A	rs74868487	0.03951
NM_001276277.3(PPIP5K2):c.3170-125T>C	rs17155121	0.03762
NM_001276277.3(PPIP5K2):c.3695C>T (p.Thr1232Met)	rs17155147	0.03664
NM_001276277.3(PPIP5K2):c.*22T>C	rs116234738	0.03174
NM_001276277.3(PPIP5K2):c.3682A>G (p.Ser1228Gly)	rs36046591	0.03161
NM_001276277.3(PPIP5K2):c.643-104T>A	rs7700471	0.02406
NM_001276277.3(PPIP5K2):c.2287-210G>T	rs58153219	0.01780
NM_001276277.3(PPIP5K2):c.3483C>T (p.Thr1161=)	rs34190293	0.01696
NM_001276277.3(PPIP5K2):c.2637+33A>G	rs112852012	0.01655
NM_001276277.3(PPIP5K2):c.1029-163C>T	rs73199713	0.01647
NM_001276277.3(PPIP5K2):c.1131-41T>G	rs34767
NM_001276277.3(PPIP5K2):c.3124A>C (p.Arg1042=)	rs26821
NM_001276277.3(PPIP5K2):c.3620-23T>G	rs154290

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