Variants in gene GRIN1 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.2444-14G>A	rs191352124	0.00024
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=)	rs145176345	0.00023
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met)	rs140672142	0.00015
NM_007327.4(GRIN1):c.1340C>A (p.Pro447His)	rs587780348	0.00014
NM_007327.4(GRIN1):c.610G>A (p.Val204Met)	rs140422926	0.00009
NM_007327.4(GRIN1):c.705C>T (p.Ala235=)	rs201343933	0.00006
NM_007327.4(GRIN1):c.1076G>A (p.Arg359His)	rs141704101	0.00004
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=)	rs146086141	0.00004
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser)	rs148008303	0.00003
NM_007327.4(GRIN1):c.2589+6G>T	rs200395927	0.00003
NM_007327.4(GRIN1):c.794-11T>A	rs1347697507	0.00002
NM_007327.4(GRIN1):c.957G>A (p.Pro319=)	rs766888803	0.00001

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