C3553587[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1705295	NM_182977.3(NNT):c.1089del (p.Leu362_Tyr363insTer)	NNT	Deletion (nonsense)	Glucocorticoid deficiency 4	GPathogenic
Select item 1687180	NM_182977.3(NNT):c.1822G>A (p.Gly608Arg)	NNT (G477R +1 more)	Single nucleotide variant (missense variant)	Glucocorticoid deficiency 4	GUncertain significance
Select item 1705519	NM_182977.3(NNT):c.2635-1G>T	NNT	Single nucleotide variant (splice acceptor variant)	Glucocorticoid deficiency 4	GPathogenic

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