List of variants in gene combination LOC105378311, PCDH15 reported as benign

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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_001384140.1(PCDH15):c.92-52T>G	rs10825347	0.50625
NM_001384140.1(PCDH15):c.157+3A>G	rs41274636	0.09581
NM_001384140.1(PCDH15):c.92-13796_92-13795insC	rs144361159	0.08987
NM_001384140.1(PCDH15):c.92-444C>T	rs11004349	0.08187
NM_001384140.1(PCDH15):c.92-165G>A	rs116415305	0.01918
NM_001384140.1(PCDH15):c.157+41381G>C	rs115394626	0.01718
NM_001384140.1(PCDH15):c.157+75G>A	rs61060705	0.01705
NM_001384140.1(PCDH15):c.92-493A>T	rs77290854	0.00896
NM_001384140.1(PCDH15):c.92-10C>T	rs202223952	0.00008
NM_001384140.1(PCDH15):c.157+198A>C	rs55733914

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