List of variants in gene POMC reported as pathogenic 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000939.4(POMC):c.-11C>A	rs753856820	0.00001
NM_000939.4(POMC):c.132+1G>A
NM_000939.4(POMC):c.313G>T (p.Glu105Ter)	rs121918111
NM_000939.4(POMC):c.403_404dup (p.Lys136fs)	rs796065035
NM_000939.4(POMC):c.416dup (p.Tyr139Ter)	rs1573250294
NM_000939.4(POMC):c.433del (p.Arg145fs)	rs796065034
NM_000939.4(POMC):c.84C>A (p.Cys28Ter)	rs1573254045
POMC, 1-BP DEL, NT6996
POMC, 1-BP INS, 6922C

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