List of variants in gene WNT1 reported as likely benign for bone development disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005430.4(WNT1):c.264T>A (p.Ser88Arg)	rs61758378	0.00373
NM_005430.4(WNT1):c.*9G>A	rs201599168	0.00041

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