List of variants in gene STX11 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_003764.4(STX11):c.*3670C>G	rs79283142	0.01181
NM_003764.4(STX11):c.*1845C>T	rs115419947	0.00646
NM_003764.4(STX11):c.*3298T>A	rs75318897	0.00321
NM_003764.4(STX11):c.*4283G>A	rs145148729	0.00321
NM_003764.4(STX11):c.546G>A (p.Glu182=)	rs146949718	0.00274
NM_003764.4(STX11):c.*4070C>A	rs148176592	0.00253
NM_003764.3(STX11):c.*4457G>A	rs59612420	0.00250
NM_003764.4(STX11):c.*1540dup	rs149740241
NM_003764.4(STX11):c.*3036ATAA[1]	rs146440209
NM_003764.4(STX11):c.*390T>C	rs79627238

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