List of variants in gene AVP reported as likely pathogenic for neurohypophyseal diabetes insipidus

Minimum submission review status:		Collection method:
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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_000490.5(AVP):c.131G>T (p.Cys44Phe)	rs1057516192
NM_000490.5(AVP):c.229GAG[1] (p.Glu78del)	rs2066119604
NM_000490.5(AVP):c.290G>A (p.Arg97His)
NM_000490.5(AVP):c.328T>A (p.Cys110Ser)

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