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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FKBP10
(M335V)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
FKBP10
Duplication
(intron variant)
Bruck syndrome 1
+4 more
GBenign/Likely benign
FKBP10
Single nucleotide variant
(intron variant)
Osteogenesis imperfecta type 11
+2 more
GBenign/Likely benign
FKBP10
(E516K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
FKBP10
(R556H)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 11
+3 more
GUncertain significance
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