List of variants reported as uncertain significance for obesity disorder by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000939.4(POMC):c.706C>G (p.Arg236Gly)	rs28932472	0.00286
NM_173598.6(KSR2):c.2512C>T (p.Arg838Cys)	rs772671793	0.00001
NM_000939.4(POMC):c.73C>T (p.Arg25Cys)
NM_005068.3(SIM1):c.475T>C (p.Ser159Pro)
NM_005068.3(SIM1):c.817G>A (p.Asp273Asn)	rs2114540224
NM_014974.3(DIP2C):c.262C>T (p.Arg88Trp)	rs965093390
NM_021969.3(NR0B2):c.712C>T (p.Arg238Cys)	rs777140276
NM_080552.3(SLC32A1):c.1121T>C (p.Leu374Pro)

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