List of variants in gene combination CAST, LOC101929710, PCSK1 reported as pathogenic for obesity disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000439.5(PCSK1):c.920C>T (p.Ser307Leu)	rs137852824	0.00001
NM_000439.5(PCSK1):c.1095+1G>A
NM_000439.5(PCSK1):c.1095+1G>T
NM_000439.5(PCSK1):c.1213C>T (p.Arg405Ter)
NM_000439.5(PCSK1):c.1350_1353del (p.Val450_Asp451insTer)
NM_000439.5(PCSK1):c.1447G>A (p.Gly483Arg)	rs137852821
NM_000439.5(PCSK1):c.238C>T (p.Arg80Ter)	rs765019354
NM_000439.5(PCSK1):c.595C>T (p.Arg199Ter)
NM_000439.5(PCSK1):c.620+4A>C	rs1580764441
NM_000439.5(PCSK1):c.638_640del (p.Ala213del)	rs137852823
NM_000439.5(PCSK1):c.748G>T (p.Glu250Ter)	rs137852822
NM_000439.5(PCSK1):c.927C>G (p.Asn309Lys)
NM_000439.5(PCSK1):c.958dup (p.Asp320fs)	rs2112419752

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