List of variants in gene MRAP reported as pathogenic for adrenocortical insufficiency

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001379228.1(MRAP):c.3G>A (p.Met1Ile)	rs80358231	0.00009
NM_001379228.1(MRAP):c.106+1G>C	rs566223651	0.00003
NM_001379228.1(MRAP):c.106+1del	rs1476574441	0.00001
NM_001379228.1(MRAP):c.106+1G>A	rs566223651
NM_001379228.1(MRAP):c.106+1G>T	rs566223651
NM_001379228.1(MRAP):c.106+3_106+4insT
NM_001379228.1(MRAP):c.17_23del (p.Asn6fs)	rs1569025178
NM_001379228.1(MRAP):c.1A>G (p.Met1Val)	rs1555897462

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