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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM177B
(H27Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM177B
(R68Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM177B
(L138S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM177B
(Y145F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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