Variants in gene SPINK1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001379610.1(SPINK1):c.174C>T (p.Cys58=)	rs35737774	0.04434
NM_001379610.1(SPINK1):c.-41G>A	rs79438751	0.03918
NM_001379610.1(SPINK1):c.194+90A>T	rs112569673	0.03151
NM_001379610.1(SPINK1):c.36G>C (p.Leu12Phe)	rs35877720	0.03139
NM_001379610.1(SPINK1):c.194+184T>A	rs114094661	0.01063
NM_001379610.1(SPINK1):c.200G>A (p.Arg67His)	rs35523678	0.01028
NM_001379610.1(SPINK1):c.231G>A (p.Gly77=)	rs34809998	0.00827
NM_001379610.1(SPINK1):c.163C>T (p.Pro55Ser)	rs111966833	0.00389
NM_001379610.1(SPINK1):c.88-23A>T	rs199929811	0.00219
NM_001379610.1(SPINK1):c.75C>T (p.Ser25=)	rs35006579	0.00133
NM_001379610.1(SPINK1):c.-22C>T	rs190219062	0.00051
NM_001379610.1(SPINK1):c.33C>T (p.Ala11=)	rs147454311	0.00048

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