List of variants in gene PIKFYVE reported as likely benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_015040.4(PIKFYVE):c.4814T>G (p.Val1605Gly)	rs61752191	0.00271
NM_015040.4(PIKFYVE):c.2535T>C (p.Ser845=)	rs138885638	0.00088
NM_015040.4(PIKFYVE):c.4156C>T (p.Arg1386Trp)	rs188498825	0.00049
NM_015040.4(PIKFYVE):c.1275C>T (p.His425=)
NM_015040.4(PIKFYVE):c.178G>A (p.Ala60Thr)
NM_015040.4(PIKFYVE):c.747T>C (p.Ser249=)

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