List of variants in gene combination MED12L, P2RY12 reported as benign by GeneDx

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022788.5(P2RY12):c.36T>G (p.Gly12=)	rs6809699	0.88072
NM_001393769.1(MED12L):c.4790+15C>T	rs10935841	0.35324
NM_022788.5(P2RY12):c.18C>T (p.Asn6=)	rs6785930	0.27022

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