List of variants reported as likely benign for obesity disorder by Fulgent Genetics, Fulgent Genetics

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_016362.5(GHRL):c.214C>A (p.Leu72Met)	rs696217	0.07013
NM_003356.4(UCP3):c.127-7C>T	rs77012485	0.00848
NM_003356.4(UCP3):c.356G>A (p.Arg119Gln)	rs17848372	0.00035
NM_003356.4(UCP3):c.72C>T (p.Ala24=)	rs70965455	0.00031
NM_006208.3(ENPP1):c.2114C>T (p.Thr705Met)	rs138032713	0.00016
NM_006208.3(ENPP1):c.750G>A (p.Pro250=)	rs368742582	0.00009
NM_006208.3(ENPP1):c.2445-5T>C	rs369942606	0.00006
NM_000439.5(PCSK1):c.352C>T (p.Leu118=)	rs750104173	0.00003
NM_006208.3(ENPP1):c.1274-5C>T	rs751500820	0.00002
NM_006208.3(ENPP1):c.2311+8A>G	rs760047831	0.00001
NM_006208.3(ENPP1):c.795+12A>G	rs1781980876	0.00001
NM_002303.6(LEPR):c.1968G>C (p.Lys656Asn)	rs1805094
NM_003356.4(UCP3):c.63C>G (p.Gly21=)	rs181883754
NM_006208.3(ENPP1):c.118C>A (p.Pro40Thr)
NM_006208.3(ENPP1):c.1437+9_1437+12del	rs376640801
NM_006208.3(ENPP1):c.313+8_313+9dup	rs377330284
NM_006208.3(ENPP1):c.313+8_313+9insTTGTGTGT	rs879243445

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