List of variants reported as uncertain significance for obesity disorder by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 8

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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.427C>T (p.Arg143Ter)	rs104894319	0.00194
NM_003356.4(UCP3):c.208C>T (p.Arg70Trp)	rs17848368	0.00007
NM_000439.5(PCSK1):c.1214G>A (p.Arg405Gln)	rs2112399256
NM_000439.5(PCSK1):c.951T>G (p.Cys317Trp)
NM_001330574.2(ZNF711):c.488T>A (p.Leu163His)
NM_003356.4(UCP3):c.126+1G>C
NM_021969.3(NR0B2):c.596T>C (p.Leu199Pro)

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