List of variants in gene UCP3 studied for obesity disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_003356.4(UCP3):c.824+1G>A	rs45476292	0.02748
NM_003356.4(UCP3):c.127-7C>T	rs77012485	0.00848
NM_003356.4(UCP3):c.427C>T (p.Arg143Ter)	rs104894319	0.00194
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_003356.4(UCP3):c.922C>T (p.Arg308Trp)	rs763155375	0.00009
NM_003356.4(UCP3):c.490G>A (p.Asp164Asn)	rs367566750	0.00008
NM_003356.4(UCP3):c.208C>T (p.Arg70Trp)	rs17848368	0.00007
NM_003356.4(UCP3):c.202A>G (p.Met68Val)	rs370829405	0.00006
NM_003356.4(UCP3):c.386T>C (p.Met129Thr)	rs1047063799	0.00004
NM_003356.4(UCP3):c.274G>A (p.Ala92Thr)	rs192655642	0.00002
NM_003356.4(UCP3):c.365C>T (p.Ala122Val)	rs773117397	0.00001
NM_003356.4(UCP3):c.126+1G>C
NM_003356.4(UCP3):c.383C>A (p.Ala128Asp)
NM_003356.4(UCP3):c.63C>G (p.Gly21=)	rs181883754

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