List of variants in gene combination LOC125418060, MRAP reported as uncertain significance for Glucocorticoid deficiency 2

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001379228.1(MRAP):c.126C>T (p.Phe42=)	rs769898813	0.00001
NM_001379228.1(MRAP):c.107-5C>T	rs373512270
NM_001379228.1(MRAP):c.206+13G>C	rs749474036

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