List of variants in gene VIPAS39 reported as likely pathogenic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001193315.2(VIPAS39):c.1048-1G>A
NM_001193315.2(VIPAS39):c.1048-1G>T
NM_001193315.2(VIPAS39):c.463_464del (p.Trp155fs)
NM_001193315.2(VIPAS39):c.618_626dup (p.Arg206_Leu208dup)	rs1594910243
NM_001193315.2(VIPAS39):c.677A>G (p.His226Arg)	rs1555366438

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