ClinVar Miner

List of variants in gene FTO reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001080432.3(FTO):c.*1380del rs5816925 0.62759
NM_001080432.3(FTO):c.*2108G>A rs708277 0.62297
NM_001080432.3(FTO):c.*721T>G rs58094871 0.03948
NM_001080432.3(FTO):c.*2301G>A rs79234192 0.02445
NM_001080432.3(FTO):c.*1860A>C rs77984007 0.01710
NM_001080432.3(FTO):c.*1315C>T rs76606072 0.01708
NM_001080432.3(FTO):c.*2334G>A rs113662449 0.01705
NM_001080432.3(FTO):c.*2180C>T rs147409759 0.01518
NM_001080432.3(FTO):c.*2249A>T rs75681401 0.01070
NM_001080432.3(FTO):c.*1082G>A rs73625209 0.00952
NM_001080432.3(FTO):c.1214C>T (p.Ala405Val) rs16952624 0.00943
NM_001080432.3(FTO):c.*1071G>C rs114521424 0.00824
NM_001080432.3(FTO):c.*619A>C rs149440289 0.00764
NM_001080432.3(FTO):c.*2551G>A rs116773044 0.00696
NM_001080432.3(FTO):c.1002T>C (p.Ile334=) rs148109727 0.00691
NM_001080432.3(FTO):c.*2442A>T rs114255834 0.00666
NM_001080432.3(FTO):c.*931C>A rs116372569 0.00640
NM_001080432.3(FTO):c.*1403C>T rs147129925 0.00188
NM_001080432.3(FTO):c.*2210A>G rs117637522 0.00095
NM_001080432.3(FTO):c.*1331G>A rs116978290 0.00087
NM_001080432.3(FTO):c.400G>A (p.Ala134Thr) rs79206939 0.00065
NM_001080432.3(FTO):c.*116C>T rs533303860 0.00015
NM_001080432.3(FTO):c.*1380G>T rs113575052
NM_001080432.3(FTO):c.*1911del rs532852190
NM_001080432.3(FTO):c.*2362G>T rs45564131

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