Variants in gene SHH with conflicting interpretations "benign" and "benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_000193.4(SHH):c.630C>T (p.Gly210=)	rs9333634	0.01171
NM_000193.4(SHH):c.570G>A (p.Ser190=)	rs9333633	0.00262
NM_000193.4(SHH):c.876G>A (p.Gly292=)	rs112055654	0.00093

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