ClinVar Miner

List of variants in gene combination MED12L, P2RY12 reported as pathogenic by Northern Blood Research Centre, University of Sydney

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_022788.5(P2RY12):c.794G>C (p.Arg265Pro)	rs755459581	0.00001

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