C3553587[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1325907	NM_182977.3(NNT):c.-26T>C	NNT	Single nucleotide variant (5 prime UTR variant)	Glucocorticoid deficiency 4 +1 more	GBenign
Select item 1174913	NM_182977.3(NNT):c.46C>T (p.Leu16=)	NNT	Single nucleotide variant (5 prime UTR variant +1 more)	Glucocorticoid deficiency 4 +1 more	GBenign
Select item 1325908	NM_182977.3(NNT):c.152-26_152-25insA	NNT	Insertion (intron variant)	Glucocorticoid deficiency 4	GBenign

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