ClinVar Miner

List of variants in gene combination PCDH12, RNF14 reported as benign by CeGaT Center for Human Genetics Tuebingen

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016580.4(PCDH12):c.240C>G (p.Asp80Glu)	rs138689340	0.01052
NM_016580.4(PCDH12):c.1743G>C (p.Val581=)	rs116711399	0.00856

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