List of variants in gene PFKM reported as likely benign by Natera, Inc.

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000289.6(PFKM):c.453G>A (p.Thr151=)	rs144370737	0.00071
NM_000289.6(PFKM):c.495T>A (p.Ile165=)	rs148858610	0.00046
NM_000289.6(PFKM):c.1653+8C>T	rs369425921	0.00022
NM_000289.6(PFKM):c.459C>T (p.Ser153=)	rs145519821	0.00021
NM_000289.6(PFKM):c.2040C>T (p.Gly680=)	rs369893708	0.00009
NM_000289.6(PFKM):c.1155C>T (p.Tyr385=)	rs146318448	0.00008
NM_000289.6(PFKM):c.1476C>T (p.Gly492=)	rs200847712	0.00005
NM_000289.6(PFKM):c.1127+10T>C	rs759084382	0.00003
NM_000289.6(PFKM):c.2265C>T (p.Tyr755=)	rs374418157	0.00003
NM_000289.6(PFKM):c.483G>A (p.Leu161=)	rs199856938	0.00001
NM_000289.6(PFKM):c.1063-6C>G	rs371033104
NM_000289.6(PFKM):c.1192-5T>C	rs778432092

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