List of variants in gene CHST14 reported as not provided for arthrogryposis syndrome

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_130468.4(CHST14):c.638G>C (p.Arg213Pro)	rs121908257	0.00001
NM_130468.4(CHST14):c.878A>G (p.Tyr293Cys)	rs121908258	0.00001
NM_130468.4(CHST14):c.1033C>T (p.Arg345Trp)	rs372422727

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