List of variants in gene PGM3 reported as benign for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_015599.3(PGM3):c.1281A>G (p.Glu427=)	rs542948	0.35441
NM_015599.3(PGM3):c.-2-190T>A	rs73749738	0.02750
NM_015599.3(PGM3):c.33A>G (p.Ala11=)	rs150763574	0.00411
NM_015599.3(PGM3):c.389+12A>T	rs150967479	0.00214
NM_015599.3(PGM3):c.1085A>T (p.Glu362Val)	rs34238319	0.00024
NM_015599.3(PGM3):c.349C>A (p.Leu117Met)	rs190279776	0.00024
NM_015599.3(PGM3):c.50A>G (p.Asn17Ser)	rs369116726	0.00002
NM_015599.3(PGM3):c.521G>T (p.Arg174Leu)	rs73749732
NM_015599.3(PGM3):c.945+13del
NM_015599.3(PGM3):c.946-7del	rs758669509

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