ClinVar Miner

List of variants in gene GRIN2B reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.1500+73G>A rs1468845 0.99423
NM_000834.5(GRIN2B):c.2360-75T>C rs4764010 0.94560
NM_000834.5(GRIN2B):c.-19+51A>C rs1421109 0.88845
NM_000834.5(GRIN2B):c.1126-73A>G rs1805199 0.75072
NM_000834.5(GRIN2B):c.2360-225T>C rs4764011 0.47590
NM_000834.5(GRIN2B):c.366C>G (p.Pro122=) rs7301328 0.41972
NM_000834.5(GRIN2B):c.3534C>T (p.His1178=) rs1806191 0.39095
NM_000834.5(GRIN2B):c.2172-176A>G rs1806194 0.30147
NM_000834.5(GRIN2B):c.1665C>T (p.Ser555=) rs1805482 0.26553
NM_000834.5(GRIN2B):c.2359+129A>G rs2072539 0.24637
NM_000834.5(GRIN2B):c.2664C>T (p.Thr888=) rs1806201 0.23527
NM_000834.5(GRIN2B):c.4197T>C (p.His1399=) rs1805247 0.16667
NM_000834.5(GRIN2B):c.1125+20A>G rs11055581 0.14832
NM_000834.5(GRIN2B):c.2359+224A>C rs2270358 0.10660
NM_000834.5(GRIN2B):c.2360-67C>T rs61216234 0.10543
NM_000834.5(GRIN2B):c.1126-240T>C rs78823315 0.09840
NM_000834.5(GRIN2B):c.2359+102G>A rs16909218 0.09786
NM_000834.5(GRIN2B):c.2359+59T>C rs16909222 0.09771
NM_000834.5(GRIN2B):c.2011-200G>T rs7312845 0.09770
NM_000834.5(GRIN2B):c.1655-231T>A rs1805527 0.09325
NM_000834.5(GRIN2B):c.2514C>T (p.Cys838=) rs3026160 0.08178
NM_000834.5(GRIN2B):c.-15G>A rs12818068 0.07885
NM_000834.5(GRIN2B):c.1126-134C>G rs1805536 0.07038
NM_000834.5(GRIN2B):c.1501-97C>T rs1805486 0.05351
NM_000834.5(GRIN2B):c.2172-299T>C rs78142938 0.05118
NM_000834.5(GRIN2B):c.2359+47C>A rs1806211 0.03870
NM_000834.5(GRIN2B):c.1126-12A>G rs76777620 0.03782
NM_000834.5(GRIN2B):c.1780+193A>G rs1805526 0.03423
NM_000834.5(GRIN2B):c.1780+78T>C rs3026175 0.03408
NM_000834.5(GRIN2B):c.15G>A (p.Ala5=) rs34315573 0.03193
NM_000834.5(GRIN2B):c.1010+196A>G rs115146194 0.02960
NM_000834.5(GRIN2B):c.2598+263A>G rs74065126 0.02747
NM_000834.5(GRIN2B):c.870C>T (p.Pro290=) rs1124894 0.02647
NM_000834.5(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246 0.02603
NM_000834.5(GRIN2B):c.504C>A (p.Ile168=) rs36031537 0.01733
NM_000834.5(GRIN2B):c.2691C>T (p.Asn897=) rs35125534 0.01112
NM_000834.5(GRIN2B):c.1341C>T (p.Asp447=) rs35025065 0.00902
NM_000834.5(GRIN2B):c.1329-32G>T rs45480400 0.00651
NM_000834.5(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931 0.00538
NM_000834.5(GRIN2B):c.-18-10G>C rs146841522 0.00215
NM_000834.5(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903 0.00206
NM_000834.5(GRIN2B):c.3117C>T (p.Tyr1039=) rs147762014 0.00123
NM_000834.5(GRIN2B):c.1781-43C>T rs181583147 0.00111
NM_000834.5(GRIN2B):c.1338A>G (p.Thr446=) rs141031272 0.00102
NM_000834.5(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818 0.00085
NM_000834.5(GRIN2B):c.1569C>T (p.Val523=) rs148573953 0.00081
NM_000834.5(GRIN2B):c.228C>T (p.Thr76=) rs77299791 0.00070
NM_000834.5(GRIN2B):c.1780+8C>T rs199986080 0.00068
NM_000834.5(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137 0.00063
NM_000834.5(GRIN2B):c.1851C>T (p.Ser617=) rs147373250 0.00045
NM_000834.5(GRIN2B):c.3389G>A (p.Arg1130Gln) rs148625092 0.00043
NM_000834.5(GRIN2B):c.4101C>T (p.Pro1367=) rs112932810 0.00043
NM_000834.5(GRIN2B):c.2010+38A>G rs201567713 0.00041
NM_000834.5(GRIN2B):c.812C>T (p.Ala271Val) rs138098032 0.00041
NM_000834.5(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966 0.00035
NM_000834.5(GRIN2B):c.45G>A (p.Val15=) rs374735893 0.00030
NM_000834.5(GRIN2B):c.2931C>G (p.Asp977Glu) rs147956755 0.00029
NM_000834.5(GRIN2B):c.3799G>T (p.Ala1267Ser) rs141844705 0.00029
NM_000834.5(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012 0.00029
NM_000834.5(GRIN2B):c.2703G>A (p.Leu901=) rs145005918 0.00026
NM_000834.5(GRIN2B):c.3549G>A (p.Thr1183=) rs201568782 0.00024
NM_000834.5(GRIN2B):c.1356C>T (p.Tyr452=) rs142935139 0.00023
NM_000834.5(GRIN2B):c.1780+9G>A rs201461091 0.00017
NM_000834.5(GRIN2B):c.2481G>A (p.Ala827=) rs189384622 0.00015
NM_000834.5(GRIN2B):c.291G>A (p.Val97=) rs202223470 0.00014
NM_000834.5(GRIN2B):c.1328+17A>G rs201560542 0.00011
NM_000834.5(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596 0.00011
NM_000834.5(GRIN2B):c.3957G>A (p.Pro1319=) rs141730031 0.00009
NM_000834.5(GRIN2B):c.4311C>T (p.Ala1437=) rs112265127 0.00009
NM_000834.5(GRIN2B):c.513C>T (p.Ile171=) rs3026183 0.00008
NM_000834.5(GRIN2B):c.1035G>A (p.Glu345=) rs146812769 0.00007
NM_000834.5(GRIN2B):c.1221C>T (p.Ser407=) rs145080218 0.00007
NM_000834.5(GRIN2B):c.2628G>A (p.Ala876=) rs199710029 0.00007
NM_000834.5(GRIN2B):c.3174C>T (p.Ser1058=) rs772364390 0.00005
NM_000834.5(GRIN2B):c.61G>A (p.Val21Met) rs79046967 0.00004
NM_000834.5(GRIN2B):c.1501-13G>A rs201829637 0.00003
NM_000834.5(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200 0.00003
NM_000834.5(GRIN2B):c.4077C>T (p.Ala1359=) rs375217280 0.00003
NM_000834.5(GRIN2B):c.834C>A (p.Ile278=) rs199835162 0.00003
NM_000834.5(GRIN2B):c.1010+37T>C rs755067488 0.00002
NM_000834.5(GRIN2B):c.1020C>T (p.Ile340=) rs778209882 0.00002
NM_000834.5(GRIN2B):c.4105G>A (p.Gly1369Ser) rs371190262 0.00002
NM_000834.5(GRIN2B):c.1125+9T>C rs764590430 0.00001
NM_000834.5(GRIN2B):c.3588T>C (p.Pro1196=) rs200884387 0.00001
NM_000834.5(GRIN2B):c.360C>T (p.Leu120=) rs377642005 0.00001
NM_000834.5(GRIN2B):c.*409T>G rs890
NM_000834.5(GRIN2B):c.-208del rs370171136
NM_000834.5(GRIN2B):c.1781-161GA[2] rs146116919
NM_000834.5(GRIN2B):c.1781-64del rs56069446
NM_000834.5(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.5(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.5(GRIN2B):c.2359+136G>A rs17822337
NM_000834.5(GRIN2B):c.2598+100T>C rs3026159
NM_000834.5(GRIN2B):c.2599-231dup rs138212867
NM_000834.5(GRIN2B):c.3796C>T (p.Pro1266Ser) rs199935748
NM_000834.5(GRIN2B):c.465C>A (p.Ser155=) rs115189840

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