List of variants in gene PCDH18 reported as likely benign

Minimum submission review status:		Collection method:
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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_019035.5(PCDH18):c.3216A>G (p.Pro1072=)	rs146591833	0.00094
NM_019035.5(PCDH18):c.2866A>G (p.Thr956Ala)	rs867545344	0.00007
NM_019035.5(PCDH18):c.1717G>A (p.Val573Ile)	rs964510877

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