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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED12L, P2RY12
(P258T)
Single nucleotide variant
(missense variant +1 more)
Platelet-type bleeding disorder 8
+3 more
GPathogenic/Likely pathogenic
MED12L, P2RY12
(R122H)
Single nucleotide variant
(missense variant +1 more)
not specified
GBenign