Variants in gene PFKM with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_000289.6(PFKM):c.41T>C (p.Ile14Thr)	rs140473672	0.00078
NM_000289.6(PFKM):c.453G>A (p.Thr151=)	rs144370737	0.00071
NM_000289.6(PFKM):c.1063-5C>T	rs758178966	0.00011
NM_000289.6(PFKM):c.2121G>A (p.Ser707=)	rs370046842	0.00011
NM_000289.6(PFKM):c.638+15C>A	rs376150217	0.00011
NM_000289.6(PFKM):c.1770C>T (p.Ala590=)	rs751097669	0.00004
NM_000289.6(PFKM):c.978G>A (p.Glu326=)	rs550083752	0.00004
NM_000289.6(PFKM):c.1005A>G (p.Val335=)	rs1454843075	0.00001
NM_000289.6(PFKM):c.1242C>G (p.Gly414=)	rs886049454	0.00001
NM_000289.6(PFKM):c.864A>G (p.Gly288=)	rs1313998695	0.00001
NM_000289.6(PFKM):c.1063-6C>A	rs371033104
NM_000289.6(PFKM):c.1063-7C>T	rs776228408
NM_000289.6(PFKM):c.1192-3_1192-2del	rs780969059

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