List of variants in gene MED12L, P2RY12 studied for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_022788.5(P2RY12):c.36T>G (p.Gly12=)	rs6809699	0.88072
NM_022788.5(P2RY12):c.365G>A (p.Arg122His)	rs778790805	0.00014
NM_022788.5(P2RY12):c.767G>A (p.Arg256Gln)	rs121917885	0.00004
NM_022788.5(P2RY12):c.772C>A (p.Pro258Thr)	rs202099742	0.00001
NM_022788.5(P2RY12):c.793C>T (p.Arg265Trp)	rs121917886	0.00001
NM_022788.5(P2RY12):c.794G>C (p.Arg265Pro)	rs755459581	0.00001
NM_022788.5(P2RY12):c.160C>T (p.Arg54Trp)
NM_022788.5(P2RY12):c.469_470del (p.Leu157fs)
NM_022788.5(P2RY12):c.662dup (p.Arg222fs)
NM_022788.5(P2RY12):c.717_718del (p.Ile240fs)	rs1560045738

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