ClinVar Miner

List of variants in gene TMEM237 reported as benign by GeneDx

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001044385.3(TMEM237):c.43-93A>T rs2540424 0.75080
NM_001044385.3(TMEM237):c.274+23A>G rs1208081 0.64988
NM_001044385.3(TMEM237):c.42+100A>G rs6723016 0.50213
NM_001044385.2(TMEM237):c.-376C>T rs11686850 0.48824
NM_001044385.3(TMEM237):c.274+266A>G rs55971100 0.45711
NM_001044385.3(TMEM237):c.1037+49C>T rs2540450 0.29727
NM_001044385.3(TMEM237):c.74+71C>T rs56321285 0.25438
NM_001044385.3(TMEM237):c.396-224G>A rs56098207 0.15252
NM_001044385.3(TMEM237):c.79+227A>G rs55754648 0.07653
NM_001044385.3(TMEM237):c.1096G>T (p.Ala366Ser) rs73989521 0.07579
NM_001044385.3(TMEM237):c.1160-170T>C rs73989519 0.07439
NM_001044385.3(TMEM237):c.42+850C>G rs2241135 0.06370
NM_001044385.3(TMEM237):c.1160-64A>G rs17384203 0.06216
NM_001044385.3(TMEM237):c.553+285C>A rs116291595 0.03599
NM_001044385.3(TMEM237):c.395+7A>G rs78297522 0.01839
NM_001044385.3(TMEM237):c.75-13T>C rs116829037 0.00764
NM_001044385.3(TMEM237):c.1037+240del rs35942565
NM_001044385.3(TMEM237):c.42+78G>C rs191676728
NM_001044385.3(TMEM237):c.42+968A>G rs79383733
NM_001044385.3(TMEM237):c.43-68G>T rs12470287
NM_001044385.3(TMEM237):c.43-73del rs370408283
NM_001044385.3(TMEM237):c.43-85dup rs370408283
NM_001044385.3(TMEM237):c.554-56del rs377654281
NM_001044385.3(TMEM237):c.870-13_870-12del rs555284377

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