List of variants in gene combination COL17A1, MIR936 reported as likely benign

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000494.4(COL17A1):c.2228-20C>A	rs367967846	0.00003
NM_000494.4(COL17A1):c.2228-14T>C	rs766323094	0.00001
NM_000494.4(COL17A1):c.2228-11T>C	rs1315899141
NM_000494.4(COL17A1):c.2228-16G>A	rs2493318940
NM_000494.4(COL17A1):c.2228-20C>G	rs367967846
NM_000494.4(COL17A1):c.2228-20C>T	rs367967846

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