ClinVar Miner

List of variants reported as likely benign for Obesity

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_138711.6(PPARG):c.1341C>T (p.His447=) rs3856806 0.11181
NM_138711.6(PPARG):c.-8-28078C>G rs1801282 0.08816
NM_016362.5(GHRL):c.214C>A (p.Leu72Met) rs696217 0.07013
NM_003356.4(UCP3):c.127-7C>T rs77012485 0.00848
NM_005912.3(MC4R):c.751A>C (p.Ile251Leu) rs52820871 0.00774
NM_138711.6(PPARG):c.1281A>G (p.Ser427=) rs41516544 0.00627
NM_000939.4(POMC):c.641A>G (p.Glu214Gly) rs80326661 0.00552
NM_000939.4(POMC):c.346C>T (p.Leu116=) rs34650613 0.00259
NM_002303.6(LEPR):c.3417A>G (p.Ala1139=) rs61781316 0.00257
NM_138711.6(PPARG):c.1362C>T (p.Ile454=) rs149367249 0.00250
NM_138711.6(PPARG):c.150C>T (p.Asp50=) rs112174008 0.00154
NM_005912.3(MC4R):c.468G>A (p.Gln156=) rs144393256 0.00060
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_002303.6(LEPR):c.3423C>T (p.Tyr1141=) rs193922651 0.00014
NM_005912.2(MC4R):c.110A>T (p.Asp37Val) rs13447325 0.00013
NM_138711.6(PPARG):c.-8-28133C>T rs200479885 0.00001
NM_003356.4(UCP3):c.63C>G (p.Gly21=) rs181883754
NM_019888.3(MC3R):c.151G>C (p.Val51Leu)

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