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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS13
(S150Y)
Single nucleotide variant
(missense variant +1 more)
Upshaw-Schulman syndrome
GUncertain significance
ADAMTS13
(N1180K +2 more)
Single nucleotide variant
(missense variant +1 more)
Upshaw-Schulman syndrome
GUncertain significance
ADAMTS13
(C1188* +2 more)
Single nucleotide variant
(nonsense +1 more)
Upshaw-Schulman syndrome
+1 more
GLikely pathogenic
ADAMTS13
(L1196P +2 more)
Single nucleotide variant
(missense variant +1 more)
Upshaw-Schulman syndrome
GUncertain significance
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