List of variants in gene POMC reported as uncertain significance for Obesity due to pro-opiomelanocortin deficiency; Inherited obesity

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000939.4(POMC):c.706C>G (p.Arg236Gly)	rs28932472	0.00286
NM_000939.4(POMC):c.583G>A (p.Ala195Thr)	rs141309351	0.00247
NM_000939.4(POMC):c.-20-675A>G
NM_000939.4(POMC):c.280AGCAGCGGC[4] (p.94SSG[4])	rs10654394

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