List of variants reported as likely pathogenic for anemia due to erythrocyte enzyme disorder by Natera, Inc.

Minimum submission review status:		Collection method:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000289.6(PFKM):c.1191+1G>A	rs746348793	0.00001
NM_000289.6(PFKM):c.1500+1G>A	rs770066278	0.00001
NM_000289.6(PFKM):c.115C>T (p.Arg39Ter)	rs1064795749
NM_000289.6(PFKM):c.116G>C (p.Arg39Pro)	rs121918193
NM_000289.6(PFKM):c.159+1G>T	rs1305706304

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