List of variants in gene VIPAS39 reported as likely benign for arthrogryposis multiplex congenita 2, neurogenic type

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_001193315.2(VIPAS39):c.632-14T>C	rs142501624	0.00164
NM_001193315.2(VIPAS39):c.-1+408G>C
NM_001193315.2(VIPAS39):c.907A>G (p.Ile303Val)

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