List of variants in gene PMM2 reported as benign by GeneDx

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000303.3(PMM2):c.67-300A>T	rs8046046	0.89511
NM_000303.3(PMM2):c.348-58_348-56dup	rs1799772	0.87127
NM_000303.3(PMM2):c.447+187A>C	rs4985001	0.85107
NM_000303.3(PMM2):c.447+147A>G	rs4985041	0.85045
NM_000303.3(PMM2):c.178+299G>C	rs2304470	0.47633
NM_000303.3(PMM2):c.178+327G>A	rs2304469	0.43498
NM_000303.3(PMM2):c.524-275C>T	rs3743809	0.41654
NM_000303.3(PMM2):c.*252C>A	rs2075828	0.41543
NM_000303.3(PMM2):c.*175G>A	rs2072688	0.26303
NM_000303.3(PMM2):c.*136A>C	rs2075827	0.24978
NM_000303.3(PMM2):c.178+142C>A	rs2304471	0.18660
NM_000303.3(PMM2):c.66+209C>T	rs9939787	0.17150
NM_000303.3(PMM2):c.639+62C>T	rs3743807	0.15368
NM_000303.3(PMM2):c.179-166A>G	rs8053440	0.15215
NM_000303.3(PMM2):c.*96G>C	rs11554040	0.14272
NM_000303.3(PMM2):c.66+180G>C	rs73501483	0.09256
NM_000303.3(PMM2):c.67-120A>T	rs12446822	0.08792
NM_000303.3(PMM2):c.255+111A>T	rs77026919	0.06244
NM_000303.3(PMM2):c.347+172C>T	rs17566708	0.04934
NM_000303.3(PMM2):c.348-101C>T	rs76295751	0.02945
NM_000303.3(PMM2):c.255+272C>T	rs113451497	0.02715
NM_000303.3(PMM2):c.590A>C (p.Glu197Ala)	rs34258285	0.02088
NM_000303.3(PMM2):c.324G>A (p.Ala108=)	rs62031146	0.01239
NM_000303.3(PMM2):c.*17G>A	rs9936097	0.00905
NM_000303.3(PMM2):c.110A>T (p.Gln37Leu)	rs2304472	0.00035
NM_000303.3(PMM2):c.179-15dup	rs145496357
NM_000303.3(PMM2):c.447+19T>C	rs11074924
NM_000303.3(PMM2):c.524-309C>A	rs3826198
NM_000303.3(PMM2):c.639+182G>T	rs9924186
NM_000303.3(PMM2):c.640-15556A>C	rs113832517
NM_000303.3(PMM2):c.640-280dup	rs3833068
NM_000303.3(PMM2):c.640-331dup	rs34609525
NM_000303.3(PMM2):c.640-332_640-331dup	rs34609525
NM_000303.3(PMM2):c.640-333_640-331dup	rs34609525

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