List of variants in gene AVP reported as pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000490.5(AVP):c.160G>C (p.Gly54Arg)	rs121964888
NM_000490.5(AVP):c.164C>T (p.Pro55Leu)	rs2517100494
NM_000490.5(AVP):c.176G>A (p.Cys59Tyr)
NM_000490.5(AVP):c.229GAG[1] (p.Glu78del)	rs2066119604
NM_000490.5(AVP):c.260C>T (p.Ser87Phe)	rs121964890
NM_000490.5(AVP):c.262G>C (p.Gly88Arg)
NM_000490.5(AVP):c.286G>T (p.Gly96Cys)
NM_000490.5(AVP):c.287G>T (p.Gly96Val)	rs121964886
NM_000490.5(AVP):c.322G>T (p.Glu108Ter)
NM_000490.5(AVP):c.55G>A (p.Ala19Thr)	rs387906511

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