Variants in gene STXBP1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001032221.6(STXBP1):c.1702+10C>T	rs147607230	0.00079
NM_001032221.6(STXBP1):c.1320C>T (p.Ile440=)	rs370249358	0.00006
NM_001032221.6(STXBP1):c.1680C>T (p.Asn560=)	rs201809337	0.00005
NM_001032221.6(STXBP1):c.299G>A (p.Arg100Gln)	rs374269726	0.00004
NM_001032221.6(STXBP1):c.1360-7C>T	rs895077278	0.00001
NM_001032221.6(STXBP1):c.144A>C (p.Thr48=)	rs1462537561
NM_001032221.6(STXBP1):c.730C>G (p.Leu244Val)	rs375972545

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