List of variants in gene AVP reported as likely benign for Inborn genetic diseases

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_000490.5(AVP):c.475G>A (p.Ala159Thr)	rs760345436	0.00080
NM_000490.5(AVP):c.127C>G (p.Pro43Ala)	rs539928673	0.00030
NM_000490.5(AVP):c.331G>A (p.Val111Met)

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