List of variants in gene VIPAS39 reported as likely benign for Arthrogryposis, renal dysfunction, and cholestasis 2

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001193315.2(VIPAS39):c.-1+408G>C	rs144902427	0.00691
NM_001193315.2(VIPAS39):c.632-14T>C	rs142501624	0.00174
NM_001193315.2(VIPAS39):c.842C>G (p.Pro281Arg)	rs151206967	0.00039
NM_001193315.2(VIPAS39):c.171C>G (p.Val57=)	rs144120903	0.00021
NM_001193315.2(VIPAS39):c.907A>G (p.Ile303Val)	rs760795319	0.00001

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