List of variants reported as benign for lethal polymalformative syndrome, Boissel type by Illumina Laboratory Services, Illumina

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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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