ClinVar Miner

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:
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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