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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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.299G>A (p.Arg100Gln)	rs2228500	0.16379
NM_000289.6(PFKM):c.306C>T (p.Ala102=)	rs11552507	0.01954
NM_000289.6(PFKM):c.594-41A>G	rs56009798	0.01863
NM_000289.6(PFKM):c.2087G>A (p.Arg696His)	rs41291971	0.01088
NM_000289.6(PFKM):c.747+24T>G	rs149600978	0.00875
NM_000289.6(PFKM):c.1338G>A (p.Gly446=)	rs150378513	0.00243
NM_000289.6(PFKM):c.2199-12A>G	rs202008060	0.00204
NM_000289.6(PFKM):c.702A>T (p.Pro234=)	rs138022863	0.00185
NM_000289.6(PFKM):c.453G>A (p.Thr151=)	rs144370737	0.00071
NM_000289.6(PFKM):c.2040C>T (p.Gly680=)	rs369893708	0.00009
NM_000289.6(PFKM):c.468G>C (p.Leu156=)	rs772301967	0.00004
NM_000289.6(PFKM):c.1467C>T (p.Asn489=)	rs753681797	0.00002
NM_000289.6(PFKM):c.888G>A (p.Leu296=)	rs753083173	0.00001

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