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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDNRA
(L48P)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
EDNRA
(Q235R)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
EDNRA
Single nucleotide variant
(synonymous variant +1 more)
Migraine with or without aura, susceptibility to, 1
+3 more
GBenign/Likely benign
TMA16, CXCL1
+537 more
Copy number gain
not provided
GPathogenic
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