List of variants in gene SCARF2 reported as likely pathogenic 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_182895.5(SCARF2):c.25del (p.Ala9fs)	rs1215759021
NM_182895.5(SCARF2):c.3G>A (p.Met1Ile)
NM_182895.5(SCARF2):c.915C>G (p.Cys305Trp)	rs1241075295

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