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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NUP155
(R1019W +2 more)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 15
GUncertain significance
LOC129993817, NUP155
(S44C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NUP155
(M391V +1 more)
Single nucleotide variant
(missense variant)
Atrial fibrillation
GUncertain significance
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