List of variants in gene combination AIP, LOC130006206 reported as benign for not provided

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_003977.4(AIP):c.132C>T (p.Asp44=)	rs11822907	0.02357
NM_003977.4(AIP):c.100-18C>T	rs202156895	0.00359
NM_003977.4(AIP):c.100-6C>A	rs539027647	0.00001

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