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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS17
Duplication
(splice acceptor variant)
Weill-Marchesani 4 syndrome, recessive
GPathogenic
ADAMTS17, LOC130058037
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic/Likely pathogenic
ADAMTS17
Single nucleotide variant
(splice donor variant)
Weill-Marchesani 4 syndrome, recessive
GPathogenic
ADAMTS17
(Q254*)
Single nucleotide variant
(nonsense)
Weill-Marchesani 4 syndrome, recessive
GPathogenic
ADAMTS17
(D218fs)
Deletion
(frameshift variant)
Weill-Marchesani 4 syndrome, recessive
GPathogenic
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