List of variants in gene INPPL1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.637A>G (p.Thr213Ala)	rs138340411	0.00053
NM_001567.4(INPPL1):c.247-6C>T	rs199604909	0.00001
NM_001567.4(INPPL1):c.2846G>A (p.Arg949Gln)	rs376511255	0.00001

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