Variants in gene SNTA1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.1426-5T>C	rs183939417	0.00221
NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly)	rs56157422	0.00217
NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu)	rs572545726	0.00198
NM_003098.3(SNTA1):c.984C>T (p.Pro328=)	rs138863915	0.00121
NM_003098.3(SNTA1):c.677G>A (p.Cys226Tyr)	rs34479952	0.00037
NM_003098.3(SNTA1):c.311-20C>T	rs200764326	0.00013
NM_003098.3(SNTA1):c.1158G>A (p.Pro386=)	rs774320273	0.00004
NM_003098.3(SNTA1):c.1437G>A (p.Leu479=)	rs780011608	0.00003
NM_003098.3(SNTA1):c.567A>T (p.Ser189=)	rs552315106

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