List of variants in gene AIP reported as uncertain significance for adrenal gland neoplasm

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003977.4(AIP):c.26G>A (p.Arg9Gln)	rs139459091	0.00037
NM_003977.4(AIP):c.827C>T (p.Ala276Val)	rs61741147	0.00009
NM_003977.4(AIP):c.355C>T (p.Arg119Trp)	rs368933035	0.00004
NM_003977.4(AIP):c.406G>T (p.Ala136Ser)	rs775549178	0.00003

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