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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCT7
(S438L +3 more)
Single nucleotide variant
(missense variant +1 more)
Myocardial infarction, susceptibility to, 1
GPathogenic
GUCY1A1
(L163fs)
Duplication
(frameshift variant +2 more)
Myocardial infarction, susceptibility to, 1
GPathogenic
LRP8
(R952Q +3 more)
Single nucleotide variant
(missense variant)
Myocardial infarction, susceptibility to, 1
Grisk factor
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